Identity
- Trade Name
- RINGFIX FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- RAD Ankle Distraction Kit; Tray FDA UDI
- Model / Reference
- 601-0014 FDA UDI
- Description
- RAD Ankle Distraction Kit; Tray FDA UDI
Identifiers
- Catalog Number
- 601-0014 FDA UDI
- Primary DI / UDI-DI
- 00886385012629 FDA UDI
- FDA Product Code
- KTT FDA UDI
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Ringfix by Stryker Corp. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 839a141d-d3ed-438c-953a-8829bb0d98c6 35 fields · synced May 31, 2026