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Moss 274524100

by Depuy Spine, Inc.

Ref 274524100Model Moss Miami Reusable Osteosynthesis Instruments

Moss 274524100 is a Class I device made by Depuy Spine, Inc., registered in EUDAMED on 15 Aug 2025 (Basic UDI-DI 0705034a001325N) and listed in FDA GUDID since 31 Dec 2016 (UDI-DI 10705034298382), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0705034a001325N Basic UDI-DI 10705034298382UDI-DIDate15 Aug 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10705034298382 UDI-DI Date31 Dec 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0705034a001325N registered 15 Aug 2025 Active
  • FDA GUDID UDI-DI 10705034298382 listed 31 Dec 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10705034298382
  2. Registered EUDAMED 0705034a001325N

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  • Withdrawn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
Moss Miami Spine System EUDAMED
Moss GUDID
Generic name
Manual orthopaedic bender, reusable
Device name
Moss Miami Rod Bender
Model / Ref / Catalog
274524100, Moss Miami Reusable Osteosynthesis Instruments
Primary DI / UDI-DI
10705034298382
Basic UDI-DI
0705034a001325N
Direct marketing DI
10705034298382
FDA product code
HXW
EMDN code
L091099 Osteosynthesis instruments, reusable - other
GMDN term
Manual orthopaedic bender, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Manual orthopaedic bender, reusable

Similar devices in this category

Other devices filed under OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Depuy Spine, Inc.

See all devices from Depuy Spine, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
Other properties (20, all answered No)