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Covera

FDA UDI

Class III (US FDA UDI)

by Angiomed GmbH & Co. Medizintechnik KG

Identity

Trade Name
COVERA FDA UDI
Generic Name
Central/peripheral venous endovascular stent-graft FDA UDI
Device Name
COVERA™ Vascular Covered Stent 8 mm x 60 mm (80 cm delivery catheter) (flared) FDA UDI
Model / Reference
AVFM08060 FDA UDI
Description
COVERA™ Vascular Covered Stent 8 mm x 60 mm (80 cm delivery catheter) (flared) FDA UDI

Identifiers

Catalog Number
AVFM08060 FDA UDI
Primary DI / UDI-DI
00801741106514 FDA UDI
FDA Product Code
PFV FDA UDI
GMDN Term
Central/peripheral venous endovascular stent-graft FDA UDI

Classification

Device Class
Class III 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Central/peripheral venous endovascular stent-graft

Covera by Angiomed GmbH & Co. Medizintechnik KG — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Central/peripheral venous endovascular stent-graft.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angiomed GmbH & Co. Medizintechnik KG

Sources (1)

  • FDA UDI ab1ab8c8-e77e-41f5-ac08-26f176ebfaba 36 fields · synced May 30, 2026