Identity
- Trade Name
- IntraBlock™ TwinStem™ FDA UDI
- Generic Name
- Diaphysis prosthesis FDA UDI
- Device Name
- IntraBlock TwinStem Rasp Size 8.75 non-sterile FDA UDI
- Model / Reference
- HI35008 FDA UDI
- Description
- IntraBlock TwinStem Rasp Size 8.75 non-sterile FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04048266007100 FDA UDI
- FDA Product Code
- HTR FDA UDI
- GMDN Term
- Diaphysis prosthesis 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
Yes
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
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
IntraBlock™ TwinStem™ by Merete GmbH — 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
- Merete GmbH
Sources (1)
- FDA UDI fbe50703-546c-49d8-8755-2851bffd218c 35 fields · synced Jun 8, 2026