Identity
- Trade Name
- GORE Hybrid Vascular Graft-CBAS FDA UDI
- Generic Name
- Synthetic vascular graft FDA UDI
- Device Name
- HYBRID VG 6-7MM X 10CM US FDA UDI
- Model / Reference
- 0650HYB0710A FDA UDI
- Description
- HYBRID VG 6-7MM X 10CM US FDA UDI
Identifiers
- Catalog Number
- 0650HYB0710A FDA UDI
- Primary DI / UDI-DI
- 00733132618903 FDA UDI
- FDA Product Code
- DSY 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
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 7 Millimeter FDA UDILength — 60 Centimeter FDA UDILumen/Inner Diameter — 6 Millimeter FDA UDI
GORE Hybrid Vascular Graft-CBAS by W. L. Gore & Associates, Inc — 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 |
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Manufacturer
- Manufacturer
- W. L. Gore & Associates, Inc
Sources (1)
- FDA UDI 8a4a8fd4-47a0-43d4-91ac-e874440c37f1 37 fields · synced May 31, 2026