Identity
- Trade Name
- IMPRA® ePTFE Vascular Grafts FDA UDI
- Generic Name
- Synthetic vascular graft FDA UDI
- Device Name
- IMPRA® ePTFE Vascular Graft, Flex™ Thinwall Small Beading, 8 mm x 10 cm FDA UDI
- Model / Reference
- F1008TWS FDA UDI
- Description
- IMPRA® ePTFE Vascular Graft, Flex™ Thinwall Small Beading, 8 mm x 10 cm FDA UDI
Identifiers
- Catalog Number
- F1008TWS FDA UDI
- Primary DI / UDI-DI
- 00801741023200 FDA UDI
- FDA Product Code
- DYF FDA UDIDSY FDA UDI
- GMDN Term
- Synthetic vascular graft FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.3450 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 10 Centimeter FDA UDI
IMPRA® ePTFE Vascular Grafts by Bard Peripheral Vascular — 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
- Bard Peripheral Vascular
Sources (1)
- FDA UDI 1dd9da69-343b-42fd-b942-1605ab31a432 37 fields · synced Jun 6, 2026