Identity
- Trade Name
- Revolution FDA UDI
- Generic Name
- Orthopaedic cement injection cannula FDA UDI
- Device Name
- Cement Mixing System with Femoral Breakaway Nozzle, Medium Solid Proximal Pressurizer, Revision Cement Restrictor, Small and Universal Cement Restrictor FDA UDI
- Model / Reference
- 0606705000S1 FDA UDI
- Description
- Cement Mixing System with Femoral Breakaway Nozzle, Medium Solid Proximal Pressurizer, Revision Cement Restrictor, Small and Universal Cement Restrictor FDA UDI
Identifiers
- Catalog Number
- 0606-705-000S1 FDA UDI
- Primary DI / UDI-DI
- 07613154354399 FDA UDI
- FDA Product Code
- OAR FDA UDI
- GMDN Term
- Orthopaedic cement injection cannula FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4200 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Orthopaedic cement injection cannula
Revolution by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 65d2d4fd-3858-47a5-b485-15a4f608ab25 35 fields · synced Jun 8, 2026