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Covera AVSL06030

by Angiomed GmbH & Co. Medizintechnik KG

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741106620 UDI-DI Date1 Aug 2018ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Covera
Generic Name
Central/peripheral venous endovascular stent-graft
Model / Ref / Catalog
AVSL06030
Description
COVERA™ Vascular Covered Stent 6 mm x 30 mm (120 cm delivery catheter) (straight)
Primary DI / UDI-DI
00801741106620
FDA Product Code
PFV
GMDN Term
Central/peripheral venous endovascular stent-graft
Device Class
Class III
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Conditional

Other devices from Angiomed GmbH & Co. Medizintechnik KG

  • Lifestent

    Class IIb

  • Highflex

    Class I

  • Covera

    Class IIb

  • Lifestent

    Class IIb

  • Covera

    Class IIb

  • Covera

    Class IIb

See all devices from Angiomed GmbH & Co. Medizintechnik KG →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No