Skip to content

Symmetry Bruns 29-5394

by Aspen Surgical Products, Inc.

Ref 29-5394

Symmetry Bruns 29-5394 is a Class I device made by Aspen Surgical Products, Inc., registered in EUDAMED on 2 Jun 2026 (Basic UDI-DI 08401132CuretteHJ) and listed in FDA GUDID since 13 Sep 2022 (UDI-DI 00887482067246), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08401132CuretteHJ Basic UDI-DI 00887482067246UDI-DIDate2 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887482067246 UDI-DI Date13 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08401132CuretteHJ registered 2 Jun 2026 Active
  • FDA GUDID UDI-DI 00887482067246 listed 13 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887482067246
  2. Registered EUDAMED 08401132CuretteHJ

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  • Withdrawn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 Bruns GUDID
Generic name
Bone curette, reusable
Device name
Curettes
Model / Ref / Catalog
29-5394
Primary DI / UDI-DI
00887482067246
Basic UDI-DI
08401132CuretteHJ
FDA product code
FZS
EMDN code
L0399 General surgery instruments, reusable - other
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 9 Inch

Related devices

Category: Bone curette, reusable

Similar devices in this category

Other devices filed under GENERAL SURGERY INSTRUMENTS, 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)