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Symmetry Meyerding 24-4560

by Aspen Surgical Products, Inc.

Ref 24-4560

Symmetry Meyerding 24-4560 is a device classified as Class I in the EU and Class II in the US made by Aspen Surgical Products, Inc., registered in EUDAMED on 2 Jun 2026 (Basic UDI-DI 08401132HandRetractorHC), cleared under FDA 510(k) K071771 on 2 Aug 2007 and listed in FDA GUDID since 28 Aug 2018 (UDI-DI 00887482061800), active (EUDAMED, FDA 510(k)), not in commercial distribution (GUDID) as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US), not in commercial distribution.

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K071771

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08401132HandRetractorHC Basic UDI-DI 00887482061800UDI-DIDate2 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887482061800 UDI-DI Date28 Aug 2018ListedStatusListed GUDID: not in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Abbreviated NumberK071771 Date2 Aug 2007DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 08401132HandRetractorHC registered 2 Jun 2026 Active
  • FDA 510(k) K071771 decided 2 Aug 2007 Active
  • FDA GUDID UDI-DI 00887482061800 listed 28 Aug 2018 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K071771
  2. Listed FDA GUDID 00887482061800
  3. Registered EUDAMED 08401132HandRetractorHC

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Symmetry ® EUDAMED
Symmetry Meyerding GUDID
Generic name
Surgical retractor/retraction system blade, reusable
Device name
Hand Retractors
Model / Ref / Catalog
24-4560
Primary DI / UDI-DI
00887482061800 EUDAMED
00887482161005 GUDID
Basic UDI-DI
08401132HandRetractorHC
510(k) Number
FDA product code
GZT
EMDN code
L03140199 Spreaders and retractors for general surgery, reusable - other
GMDN term
Surgical retractor/retraction system blade, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
Not in Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00887482061800
GUDID
00887482161005
Device classEUDAMED
Class I
GUDID
Class II

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00887482061800; FDA GUDID lists 00887482161005), so their flags are not compared. Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Cleared under the same submission (K071771)

and 8 more cleared under K071771

Similar devices in this category

Other devices filed under SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER.

Other devices from Aspen Surgical Products, Inc.

See all devices from Aspen Surgical Products, Inc. →

Properties

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