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Symmetry Fork 62-0712

by Aspen Surgical Products, Inc.

Ref 62-0712

Symmetry Fork 62-0712 is a Class I device made by Aspen Surgical Products, Inc., registered in EUDAMED on 28 Aug 2026 (Basic UDI-DI 08401132ForkP7) and listed in FDA GUDID since 16 Aug 2024 (UDI-DI 00887482116616), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08401132ForkP7 Basic UDI-DI 00887482116616UDI-DIDate28 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887482116616 UDI-DI Date16 Aug 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08401132ForkP7 registered 28 Aug 2026 Active
  • FDA GUDID UDI-DI 00887482116616 listed 16 Aug 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887482116616
  2. Registered EUDAMED 08401132ForkP7

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Symmetry® EUDAMED
Symmetry Fork GUDID
Generic name
Tuning fork
Device name
Tuning Forks
Model / Ref / Catalog
62-0712
Primary DI / UDI-DI
00887482116616
Basic UDI-DI
08401132ForkP7
FDA product code
GWX
EMDN code
Z12040105 Perception threshold equipment
GMDN term
Tuning fork
Device class
Class I
Regulation number
882.1525
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Other devices filed under GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)