Identity
- Trade Name
- RFS Instrument FDA UDI
- Generic Name
- Orthopaedic bone wire FDA UDI
- Device Name
- RFS™ K-Wire 1.60 x 15 Threaded FDA UDI
- Model / Reference
- RFS-CKW160 FDA UDI
- Description
- RFS™ K-Wire 1.60 x 15 Threaded FDA UDI
Identifiers
- Catalog Number
- RFS-CKW160 FDA UDI
- Primary DI / UDI-DI
- E302RFSCKW1609 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Orthopaedic bone wire FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
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
Dimensions & Sizes
- Size
- Length — 150 Millimeter FDA UDIWidth — 1.6 Millimeter FDA UDI
RFS Instrument by Bioretec Oy — 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
- Bioretec Oy
Sources (1)
- FDA UDI eb2c075b-218c-4485-9489-f246859d6817 37 fields · synced May 30, 2026