Identity
- Trade Name
- Uni-frame® Thermoplastic FDA UDI
- Generic Name
- Patient positioning thermoplastic mould material FDA UDI
- Device Name
- 25.4cm IMRT Style 18 thermoplastic (2.4mm) FDA UDI
- Model / Reference
- MTAPUI1824 FDA UDI
- Description
- 25.4cm IMRT Style 18 thermoplastic (2.4mm) FDA UDI
Identifiers
- Catalog Number
- MTAPUI1824 FDA UDI
- Primary DI / UDI-DI
- 10841439103545 FDA UDI
- FDA Product Code
- LNH FDA UDIIYE FDA UDI
- GMDN Term
- Patient positioning thermoplastic mould material FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1000 FDA UDI892.5050 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
MR Safe FDA UDI
Category: Patient positioning thermoplastic mould material
Uni-frame® Thermoplastic by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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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
- Medtec LLC
Sources (1)
- FDA UDI 32f00c09-8a4c-4285-ac35-bad5d138f8ff 37 fields · synced Jun 8, 2026