Making Success: The Standard
Making Success: The Standard
Making success
the standard
ENT solutions
Balloon dilation
XprESS ENT dilation system 02
Nasal implants
LATERA absorbable nasal implant system 03
Cryotherapy
ClariFix cryotherapy system 04
Bioresorbable dressings
NasoPore bioresorbable nasal dressing* 05
HemoPore nasal dressing* 06
XeroGel nasal/epistaxis pack* 06
OtoPore bioresorbable ear dressing* 07
Navigation
Stryker ENT navigation system powered by Scopis software 08
Visualization
FocESS image solutions 10
FocESS sinuscopes 11
Surgical instruments
Entellus Medical shaver system and blades 12
Entellus Medical shaver system components 13
ESSx microdebrider* 14
MiniFESS turbinate forceps 15
MiniFESS Blakesley thru-cut forceps 16
MiniFESS Blakesley forceps 17
MiniFESS Takahashi forceps 18
MiniFESS sickle knife 19
MiniFESS maxillary seekers 20
MiniFESS sphenoid seeker/freer 21
MiniFESS Light Seeker sinus confirmation tool 22
MiniFESS surgical instrumentation 23
Reinforced anesthesia needle 24
Cliq suction pump 25
Cyclone sinonasal suction and irrigation system 26
ENT ordering information
Navigation consumables Call: 866 620 7615 | Fax: 866 620 7616 | [email protected]
Fiagon ENT navigation system consumables 27 *To order bioresorbable dressings and ESSx microdebrider, please contact Stryker instruments
LATERA
delivery device
XprESS Ultra
ENT dilation system
XprESS LoProfile
ENT dilation system
Product image is representative only and will include size markings on both the delivery device and implant tray.
Note: 1 system includes: 1 balloon dilation device, 1 syringe, 1 extension line, 1 bending tool
XprESS ENT dilation system Indication for Use: To access and treat the maxillary ostia/ethmoid infundibula in patients 2 years and older, and frontal ostia/recesses and
sphenoid sinus ostia in patients 12 years and older using a transnasal approach. The bony sinus outflow tracts are remodeled by balloon displacement of adjacent bone and
paranasal sinus structures.
To dilate the cartilaginous portion of the Eustachian tube for treating persistent Eustachian tube dysfunction in patients 18 years and older using a transnasal approach.
Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
LATERA system Instructions for Use: The LATERA absorbable nasal implant is indicated for supporting upper and lower lateral nasal cartilage.
A physician using XprESS for Eustachian tube dilation must either have: (i) experience with a Eustachian tube balloon dilation device or (ii) undergone cadaver training on the
use of a balloon dilation device for Eustachian tube dilation. If a physician who intends to use XprESS for Eustachian tube dilation does not meet at least one of these criteria, Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events.
please contact your Stryker representative to arrange training. Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
2 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 3
Cryotherapy Bioresorbable dressings
NasoPore
nasal dressing
NasoPore FD bioresorbable nasal packing Indications for Use: NasoPore FD is a fragmentable nasal dressing and is indicated for use in patients undergoing nasal/sinus
surgery as a space occupying stent to separate and prevent adhesion between mucosal surfaces; to help control minimal bleeding following surgery or nasal trauma by tamponade
effect and blood absorption.
The dressing is a biodegradable, polyurethane foam that fragments within several days. The nasal dressing drains from the nasal cavity via natural mucus flow and/or irrigation.
NasoPore bioresorbable nasal packing Indications for Use: Nasopore is a fragmentable nasal dressing and is indicated for use in patients undergoing nasal/sinus surgery as
a space occupying stent to separate and prevent adhesions between mucosal surfaces; to help control minimal bleeding following surgery or nasal trauma by tamponade effect and
blood absorption.
The dressing is a biodegradable, polyurethane foam that fragments within several days. The nasal dressing drains from the nasal cavity via natural mucus flow.
NasoPore bioresorbable nasal packing contraindications: This product is contraindicated for surgical implantation.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
ClariFix device Indications for Use: The ClariFix device is intended to be used as a cryosurgical tool for the destruction of unwanted tissue during surgical procedures,
including in adults with chronic rhinitis.
Most common side effects associated with the ClariFix treatment are temporary increased congestion and transient pain or discomfort, including headache. To order bioresorbable dressings, please contact Stryker instruments
Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events. Call: 800 253 3210 | Fax: 866 531 1393 | [email protected]
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
4 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 5
Bioresorbable dressings Bioresorbable dressings
Otopore square
ear dressing
HemoPore
nasal dressing
HemoPore fragmentable nasal dressing Indications for Use: HemoPore is intended for use in patients undergoing nasal/sinus surgery as a temporary wound dressing.
HemoPore functions as a topical hemostatic aid to control mild bleeding by tamponade effect, blood absorption, platelet activation and aggregation. It acts as an adjunct to aid
in the natural healing process as a space occupying stent to separate and support tissues. It prevents adhesions and minimizes edema. HemoPore is indicated for use as a nasal
packing to treat epistaxis.
The dressing is a biodegradable, polyurethane foam that fragments within several days. The nasal dressing drains from the nasal cavity via natural mucus flow and/or irrigation.
HemoPore fragmentable nasal dressing contraindications: HemoPore should not be used on patients who have known allergies to shellfish.
XeroGel nasal/epistaxis pack Indications for Use: XeroGel dressing is indicated for use in patients undergoing nasal/sinus surgery as a space-occupying packing to:
• separate tissue or structures compromised by surgical trauma
• separate and prevent adhesions between mucosal surfaces; including during mesothelial cell regeneration in the nasal cavity
• help control minimal bleeding following surgery or trauma
• help control minimal bleeding following surgery or trauma by tamponade effect, blood absorption and platelet aggregation
• act as an adjunct to aid in the natural healing process OtoPore fragmentable ear dressing Indications for Use: OtoPore is a fragmentable ear packing and is indicated for use in patients undergoing ear surgery as a space
occupying stent to separate and prevent adhesions between mucosal surfaces; to help control minimal bleeding following ear surgery by tamponade effect and blood absorption.
XeroGel dressing is indicated for use as a nasal packing to treat epistaxis.
XeroGel nasal/epistaxis pack Contraindications: This product is contraindicated for use in patients with a known hypersensitivity/allergy to shellfish. OtoPore fragmentable ear dressing Contraindications: This product is contraindicated for surgical implantation.
Refer to XeroGel dressing Instructions for Use (IFU) for a complete listing of precautions and possible adverse effects. Refer to OtoPore fragmentable ear dressing Instructions for Use (IFU) for a complete listing of precautions and possible adverse effects.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
To order bioresorbable dressings, please contact Stryker instruments To order bioresorbable dressings, please contact Stryker instruments
Call: 800 253 3210 | Fax: 866 531 1393 | [email protected] Call: 800 253 3210 | Fax: 866 531 1393 | [email protected]
6 7
Navigation Navigation
Headrest - adapter B package 8000-012-005 TGS universal headrest, mounting arm, adapter B, 0.25" x 2.5" Precision pointer electromagnetic 8000-050-001 1.5 mm, malleable
Headrest - adapter C package 8000-013-005 TGS universal headrest, mounting arm, adapter C, 0.25" x 3.25" Registration pointer electromagnetic 8000-050-003 2.5 mm
Suction tube, Frazier electromagnetic 8000-050-005 3 mm, malleable, straight suction
Suction tube, Eicken electromagnetic 8000-050-006 3 mm, malleable, curved suction
Indications for Use: The Stryker ENT navigation system EM and the TGS Guidewire and updated Scopis software are indicated for any medical condition in
which the use of stereotactic surgery may be appropriate, and where reference to a rigid anatomical structure in the field of ENT surgery, such as the paranasal Endoscope tracker electromagnetic 8000-060-001 Navigation of compatible 0°, 30° and 45° endoscopes
sinuses, mastoid anatomy, can be identified relative to a CT or MR based model of the anatomy. with 4 mm diameter and 175 mm length
Example procedures include, but are not limited to the following ENT procedures:
Calibration body electromagnetic 8000-060-002 Calibration of compatible 0°, 30° and 45° endoscopes
• Transsphenoidal access procedures;
• Intranasal procedures;
4 mm diameter
• Sinus procedures, such as Maxillary antrostomies, Ethmoidectomies, Sphenoidotomies/Sphenoid explorations, Turbinate resections, and Frontal sinusotomies; Universal tracker electromagnetic 8000-060-006 Allows navigation of a variety of typical FESS instruments
• ENT related anterior skull base procedures in combination with the instrument adapter system
Instrument clip electromagnetic 8000-060-030 4 mm
Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events as well as cleaning, sterilizing and care for surgical instruments.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
8 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 9
Visualization Visualization
0˚ 30˚ 45˚
FocESS
sinuscopes
FocESS HD
wireless camera
FocESS
sterilization tray
FocESS sinuscope Indications for Use: The FocESS sinuscope is intended to provide the physician with a means for endoscopic diagnostic and therapeutic sinus surgical
procedures. The Sinuscope is indicated for use in, but not limited to such procedures as examination of sinus passages and cavities, and removal of abnormal growths such as
polyps and facio-plastic surgery.
FocESS HD wireless camera Indications for Use: The FocESS HD wireless camera is indicated for use in endoscopic procedures to allow visualization of the nasal and sinus
cavities when used with an appropriately indicated endoscope. FocESS sinuscope sterilization tray Indications for Use: The FocESS sinuscope sterilization tray is used to organize and protect the FocESS sinuscopes that are sterilized
by a healthcare provider. The FocESS sinuscope sterilization tray is intended to allow sterilization of the enclosed medical devices during these sterilization cycles: pre-vacuum
Intended Use: The FocESS HD wireless camera is intended for use in a physician’s office during endoscopic sinus examinations and procedures. The wireless camera is not steam, STERRAD 100S Standard, STERRAD 100NX Standard, ethylene oxide, STERRAD NX Standard, STERRAD 100NX Express. The tray is intended to be used in conjunction
intended for used in the sterile field. with a legally marketed wrap. The tray is not intended on its own to maintain sterility.
Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events as well as cleaning, sterilizing and care. Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events as well as cleaning, sterilizing and care.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
10 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 11
Surgical instruments Surgical instruments
Shaver system console 4 mm double serrated 40° curved blade Foot pedal Lubricant and
cleaning fluid
Entellus Medical shaver system Indications for Use: The Entellus Medical shaver system has been designed for shaping bone and for the resection of soft and hard tissues Entellus Medical shaver system Indications for Use: The Entellus medical shaver system has been designed for shaping bone and for the resection of soft and hard tissues
as part of surgical procedures in the areas of otorhinolaryngology. as part of surgical procedures in the areas of otorhinolaryngology.
Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events as well as cleaning, sterilizing and care for surgical instruments. Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events as well as cleaning, sterilizing and care for surgical instruments.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
12 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 13
Surgical instruments Surgical instruments
ESSx microdebrider
Microdebrider blades
Aggressive blade 5290-011-000 4.0 mm, 11 cm, 5-pack
Aggressive serrated blade 5290-435-100 3.5 mm, 11 cm, 40˚, 5-pack
Aggressive serrated blade 5290-440-100 4.0 mm, 11 cm, 40˚, 5-pack
Jaguar blade 5290-530-000 3.5 mm, 8c m 5-pack
Jaguar blade 5290-540-000 4.0 mm, 8 cm, 5-pack
Aggressive serrated blade 5290-628-000 2.5 mm, 8 cm, 5-pack
Aggressive serrated blade 5290-635-000 3.5 mm, 8 cm, 5-pack
ESSx microdebrider Indications for Use: For use with the Stryker Consolidated Operating Room Equipment (CORE) system software revision 6.1 or higher. The handpiece
is designed for use in endoscopic or open plastic, reconstructive, and aesthetic surgery of the head and neck.
Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events as well as cleaning, sterilizing and care for surgical instruments.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
Call: 800 253 3210 | Fax: 866 531 1393 | [email protected] Please see instructions for cleaning, sterilizing and care for surgical instruments.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
14 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 15
Surgical instruments Surgical instruments
Please see instructions for cleaning, sterilizing and care for surgical instruments. Please see instructions for cleaning, sterilizing and care for surgical instruments.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
16 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 17
Surgical instruments Surgical instruments
Straight
Please see instructions for cleaning, sterilizing and care for surgical instruments. Please see instructions for cleaning, sterilizing and care for surgical instruments.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
18 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 19
Surgical instruments Surgical instruments
Angle: 78˚
Connections: Wolf adapter Storz adapter Portable red LED light source
ACMI, Wolf and Storz
MiniFESS Light Seeker Indications for Use: The Light Seeker is intended to locate, illuminate within, and transilluminate across nasal and sinus structures, including the
frontal, ethmoid and maxillary sinuses, in patients aged 18 and over.
Portable red LED light source Indication for Use: The Portable red LED light source is indicated for use in endoscopic procedures to locate, illuminate within and
transilluminate across nasal and sinus structures when used with the MiniFESS Light Seeker.
Portable red LED light source Intended Use: The Portable red LED light source is intended for use in a physician’s office during endoscopic procedures. The Portable red
LED light source is not intended for use in the sterile field.
Please see instructions for cleaning, sterilizing and care for surgical instruments. Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
20 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 21
Surgical instruments Surgical instruments
Reinforced
anesthesia needle
MiniFESS Light Seeker Indications for Use: The Light Seeker is intended to locate, illuminate within and transilluminate across nasal and sinus structures, including the
frontal, ethmoid and maxillary sinuses, in patients aged 18 and over.
MiniFESS sterilization tray Indications for Use: The MiniFESS sterilization tray is used to organize and protect the MiniFESS instruments that are sterilized by a
healthcare provider. The MiniFESS sterilization tray is intended to allow sterilization of the enclosed medical devices during a pre-vacuum steam sterilization cycle.
The tray is intended to be used in conjunction with a legally marketed wrap. The tray is not intended on its own to maintain sterility. Reinforced anesthesia needle Indications for Use: For use in injecting local anesthetics into a patient to provide regional anesthesia.
Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events as well as cleaning, sterilizing and care for surgical instruments. Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. Caution: Federal (USA) law restricts these devices to sale by or on the order of a physician.
22 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 23
Surgical instruments Surgical instruments
Cliq suction
pump
Please see instructions for cleaning, sterilizing and care for surgical instruments.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
24 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 25
Surgical instruments Navigation
Cyclone device
GuideWire
and bending tool
device
26 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 27
28 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | [email protected] 29
ENT ordering information
*To order bioresorbable dressings and ESSx microdebrider, please contact Stryker instruments
ENT
See Instructions for Use - visit: https://ent.stryker.com/physician-resources/instructions-for-use Stryker ENT
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
3600 Holly Lane North, Suite 40
This document is intended solely for the use of healthcare professionals. A surgeon must always rely on his or her own professional clinical Plymouth, MN 55447
judgment when deciding whether to use a particular product when treating a particular patient. We do not dispense medical advice and O 866 620 7615
recommend that surgeons be trained in the use of any particular product before using it in surgery. F 763 463 1599
The information presented is intended to demonstrate Stryker’s products. A surgeon must always refer to the package insert, product label and/
or instructions for use, including the instructions for cleaning and sterilization (if applicable), before using any of Stryker’s products. Products
may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets.
Please contact your representative if you have questions about the availability of Stryker’s products in your area.
Stryker or its affiliated entities own, use, or have applied for the following trademarks or service marks: Building Blocks, ClariFix, Cyclone,
Entellus Medical, ESSx, FocESS, HemoPore, LATERA, Light Seeker, MiniFESS, NasoPore, OtoPore, Scopis, Stryker, TGS, XeroGel and XprESS. All
other trademarks are trademarks of their respective owners or holders.
The absence of a product, feature, or service name, or logo from this list does not constitute a waiver of Stryker’s trademark or other intellectual
property rights concerning that name or logo.
4278-018 rD 02/2020
Copyright © 2020 Stryker ent.stryker.com