the standard - ENT Stryker

1 Making success the standardENT solutionsENT ordering informationCall: 866 620 7615 | Fax: 866 620 7616 | *To order bioresorbable dressings and ESSx microdebrider, please contact Stryker instrumentsCall: 800 253 3210 | Fax: 866 531 1393 | Balloon dilationXprESS ENT dilation system02 Nasal implantsLATERA absorbable nasal implant system03 CryotherapyClariFix cryotherapy system04 Bioresorbable dressingsNasoPore bioresorbable nasal dressing*05 HemoPore nasal dressing*06 XeroGel nasal/epistaxis pack*06 OtoPore bioresorbable ear dressing*07 NavigationStryker ENT navigation system powered by Scopis software08 VisualizationFocESS image solutions10 FocESS sinuscopes11 Surgical instrumentsEntellus Medical shaver system and blades12 Entellus Medical shaver system components13 ESSx microdebrider*14 MiniFESS turbinate forceps 15 MiniFESS Blakesley thru-cut forceps16 MiniFESS Blakesley forceps17 MiniFESS Takahashi

2 Forceps18 MiniFESS sickle knife19 MiniFESS maxillary seekers20 MiniFESS sphenoid seeker/freer21 MiniFESS Light Seeker sinus confirmation tool22 MiniFESS surgical instrumentation23 Reinforced anesthesia needle 24 Cliq suction pump 25 Cyclone sinonasal suction and irrigation system26 Navigation consumablesFiagon ENT navigation system consumables27 ENT solutions1To order, please call 866 620 761523 Ordering information | Call: 866 620 7615 | Fax: 866 620 7616 | ENT dilation systemXprESS 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.

3 The bony sinus outflow tracts are remodeled by balloon displacement of adjacent bone and paranasal sinus dilate the cartilaginous portion of the Eustachian tube for treating persistent Eustachian tube dysfunction in patients 18 years and older using a transnasal 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 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 contact your Stryker representative to arrange dilationProductCatalog LoProfile systemLPLF-1055x20 mm, 1 systemXprESS LoProfile systemLPLF-1066x20 mm, 1 systemXprESS LoProfile systemLPLF-1077x20 mm, 1 systemXprESS LoProfile systemLPLF-2055x8 mm, 1 systemXprESS LoProfile systemLPLF-2066x8 mm, 1 systemXprESS Ultra systemU L F-1055x20 mm, 1 systemXprESS Ultra systemU L F-1066x20 mm, 1 systemXprESS Ultra systemULF-2055x8 mm.

4 1 systemXprESS Ultra ENT dilation systemLATERA delivery deviceXprESS LoProfile ENT dilation systemLATERA implant tray and absorbable nasal implantsLATERA system Instructions for Use: The LATERA absorbable nasal implant is indicated for supporting upper and lower lateral nasal cartilage. 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 absorbable nasal implant systemNasal implantsProductOrder implant system20 LATSYS01 20 mm, 1 systemLATERA implant system20 LATSYS0320 mm, 3 systemsLATERA implant system20 LATSYS20 mm, 6 systemsLATERA implant systemL ATSYS01 24 mm, 1 systemLATERA implant systemLATSYS0324 mm, 3 systemsLATERA implant systemLATSYS24 mm, 6 systemsNote: 1 system includes: 1 implant delivery device, 2 absorbable nasal implants XprESS Ultra system ULF-206 6x8 mm, 1 system Note: 1 system includes: 1 balloon dilation device, 1 syringe, 1 extension line, 1 bending tool Product image is representative only and will include size markings on both the delivery device and implant information | Call.

5 866 620 7615 | Fax: 866 620 7616 | 5 ClariFix cryotherapy systemCryotherapyProductCatalog systemCFX-1000 Includes: 1 cryotherapy device and 2 cryo canistersClariFix cryo canisterCF X-100210 mL nitrous oxide canister for ClariFix deviceClariFix 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. Please see Instructions for Use (IFU) for a complete listing of warnings, precautions and adverse events.

6 Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. ProductCatalog dressing5400-010-004 standard , 4 cm, 8-packNasoPore dressing5400-010-008 standard , 8 cm, 8-packNasoPore dressing5400-020-004 Firm, 4 cm, 8-packNasoPore dressing5400-020-008 Firm, 8 cm, 8-packNasoPore dressing5400-030-004 Extra firm, 4 cm, 8-packNasoPore dressing5400-030-008 Extra firm, 8 cm, 8-packNasoPore FD dressing5400-020-108 Fast degrading, 8 cm, 8-packNasoPore bioresorbable nasal dressingBioresorbable dressingsNasoPore 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.

7 To help control minimal bleeding following surgery or nasal trauma by tamponade effect and blood 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 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 dressing is a biodegradable, polyurethane foam that fragments within several days. The nasal dressing drains from the nasal cavity via natural mucus bioresorbable nasal packing contraindications: This product is contraindicated for surgical : Federal (USA) law restricts this device to sale by or on the order of a nasal dressingNasoPore FD nasal dressingClariFix cryotherapy deviceTo order bioresorbable dressings, please contact Stryker instrumentsCall: 800 253 3210 | Fax: 866 531 1393 | 67 Hemostatic with chitosanBioresorbable dressingsHemoPore fragmentable nasal dressing Indications for Use: HemoPore is intended for use in patients undergoing nasal/sinus surgery as a temporary wound dressing.

8 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 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 fragmentable nasal dressing contraindications: HemoPore should not be used on patients who have known allergies to 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.

9 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 processXeroGel dressing is indicated for use as a nasal packing to treat nasal/epistaxis pack Contraindications: This product is contraindicated for use in patients with a known hypersensitivity/allergy to shellfish. Refer to XeroGel dressing Instructions for Use (IFU) for a complete listing of precautions and possible adverse : Federal (USA) law restricts this device to sale by or on the order of a nasal packHemoPore nasal dressingProductCatalog nasal dressingHemoPore dressing5400-020-2088 cm, 8-packXeroGel nasal/epistaxis packXeroGel packXG -102 L x W x cm thick, box of 2 individual sterile unitsXeroGel packXG -108 L x W x cm thick, box of 8 individual sterile unitsProductCatalog dressing5400-010-000 Cylinder, standard , 2 x 1 cm, 8-packOtoPore dressing5400-020-000 Cylinder, firm, 2 x 1 cm, 8-packOtoPore dressing5400-020-100 Square, firm, L x W x cm thick, 8-packOtoPore bioresorbable ear dressingBioresorbable dressingsOtoPore fragmentable ear dressing Indications for Use.

10 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 fragmentable ear dressing Contraindications: This product is contraindicated for surgical 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. Otopore cylinder ear dressingOtopore square ear dressingTo order bioresorbable dressings, please contact Stryker instrumentsCall: 800 253 3210 | Fax: 866 531 1393 | To order bioresorbable dressings, please contact Stryker instrumentsCall: 800 253 3210 | Fax: 866 531 1393 | 89 Ordering information | Call: 866 620 7615 | Fax.