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Symmetry Quickert 60-2100

by Aspen Surgical Products, Inc.

Part of a family of 78 devices: see the family page

Ref 60-2100

Symmetry Quickert 60-2100 is a Class I device made by Aspen Surgical Products, Inc., registered in EUDAMED on 15 Jul 2026 (Basic UDI-DI 08401132ProbeTP) and listed in FDA GUDID since 28 Sep 2022 (UDI-DI 00887482111543), 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 Number08401132ProbeTP Basic UDI-DI 00887482111543UDI-DIDate15 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887482111543 UDI-DI Date28 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08401132ProbeTP registered 15 Jul 2026 Active
  • FDA GUDID UDI-DI 00887482111543 listed 28 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887482111543
  2. Registered EUDAMED 08401132ProbeTP

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  • Withdrawn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 Quickert GUDID
Generic name
Ophthalmic surgical probe, reusable
Device name
Surgical Probes
Model / Ref / Catalog
60-2100
Primary DI / UDI-DI
00887482111543
Basic UDI-DI
08401132ProbeTP
FDA product code
HNL
EMDN code
L031102 Exploration probes, reusable
GMDN term
Ophthalmic surgical probe, reusable
Device class
Class I
Regulation number
886.4350
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ophthalmic surgical probe, reusable

Similar devices in this category

Other devices filed under EXPLORATION PROBES, REUSABLE.

Other devices from Aspen Surgical Products, Inc.

See all devices from Aspen Surgical Products, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)