Identity
- Trade Name
- Stryker Tourniquet FDA UDI
- Generic Name
- Tourniquet cuff, reprocessed FDA UDI
- Device Name
- Stryker Color Cuff II Adt 30x4in. 5921-030-135 FDA UDI
- Model / Reference
- RM-5921-024-135 FDA UDI
- Description
- Stryker Color Cuff II Adt 30x4in. 5921-030-135 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00816317022648 FDA UDI
- FDA Product Code
- KCY FDA UDI
- GMDN Term
- Tourniquet cuff, reprocessed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.5910 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Stryker Tourniquet by Renu Medical, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Renu Medical, Inc
Sources (1)
- FDA UDI 9eebd255-fd6c-421c-be50-f3084d7f654b 34 fields · synced Jun 1, 2026