Identity
- Trade Name
- RFS Instrument FDA UDI
- Generic Name
- Bone tap, reusable FDA UDI
- Device Name
- RFS™ Cannulated TAP 3.5 FDA UDI
- Model / Reference
- RFS-CTA35 FDA UDI
- Description
- RFS™ Cannulated TAP 3.5 FDA UDI
Identifiers
- Catalog Number
- RFS-CTA35 FDA UDI
- Primary DI / UDI-DI
- E302RFSCTA359 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Bone tap, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
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 6e084643-ad67-418e-b570-619a8a2d0adf 36 fields · synced May 31, 2026