Identity
- Trade Name
- VECTRA®, VASCULAR ACCESS GRAFT FDA UDI
- Generic Name
- Arteriovenous shunt FDA UDI
- Model / Reference
- 10002-6020-003 FDA UDI
Identifiers
- Catalog Number
- 10002-6020-003 FDA UDI
- Primary DI / UDI-DI
- 00813024011439 FDA UDI
- FDA Product Code
- DSY FDA UDI
- GMDN Term
- Arteriovenous shunt FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.3450 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Category: Arteriovenous shunt
Vectra®, Vascular Access Graft by Thoratec Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Arteriovenous shunt.
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- HeRO® — Merit Medical Systems, Inc. · Class II
- CLEARVIEW® — MEDTRONIC, INC. · Class II
- HeRO® — Merit Medical Systems, Inc. · Class II
- Artegraft Vascular Graft — LeMaitre Vascular, Inc. · Class III
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
- Thoratec Corp
Sources (1)
- FDA UDI c2f4c369-b9aa-4794-98df-8d779e2a4840 35 fields · synced May 31, 2026