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Anchorsure A-SURE

by Desarrollo E Investigacion Medica Aragonesa Sl

Anchorsure A-SURE is a Class II device made by Desarrollo E Investigacion Medica Aragonesa Sl, listed in FDA GUDID since 19 Oct 2020 (UDI-DI 08437007606904), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08437007606904 UDI-DI Date19 Oct 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Anchorsure
Generic name
Soft-tissue/mesh anchor, non-bioabsorbable
Model / reference
A-SURE
Primary DI / UDI-DI
08437007606904
FDA product code
PBQ
GMDN term
Soft-tissue/mesh anchor, non-bioabsorbable
Device class
Class II
Regulation number
884.4530
GUDID distribution status
In Commercial Distribution

Related devices

Category: Soft-tissue/mesh anchor, non-bioabsorbable

Similar devices in this category

Other devices filed under Soft-tissue/mesh anchor, non-bioabsorbable.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (9, all answered No)