Identity
- Trade Name
- OsteoBridge™ Interlocking screw FDA UDI
- Generic Name
- Diaphysis prosthesis FDA UDI
- Model / Reference
- 5.0 52 FDA UDI
Identifiers
- Catalog Number
- GB35052 FDA UDI
- Primary DI / UDI-DI
- 04048266000750 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Diaphysis prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3020 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Dimensions & Sizes
- Size
- Length — 52 Millimeter FDA UDIOuter Diameter — 5 Millimeter FDA UDI
OsteoBridge™ Interlocking screw by Merete GmbH — 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Merete GmbH
Sources (1)
- FDA UDI 846bcc70-a5b0-49dc-804d-a7ca71ac7e7c 36 fields · synced May 30, 2026