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naturesQue MaxOss P 58491

by Collagen Matrix, Inc.

Ref 58491

naturesQue MaxOss P 58491 is a device classified as Class III in the EU and Class II in the US made by Collagen Matrix, Inc., registered in EUDAMED on 30 Jun 2026 (Basic UDI-DI B-00813954023458) and listed in FDA GUDID since 25 Feb 2020 (UDI-DI 00813954023458), active as of 23 Oct 2026.

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

CE MDD

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00813954023458 Basic UDI-DI 00813954023458UDI-DIDate30 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00813954023458 UDI-DI Date25 Feb 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00813954023458 registered 30 Jun 2026 Active
  • FDA GUDID UDI-DI 00813954023458 listed 25 Feb 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00813954023458
  2. Registered EUDAMED B-00813954023458

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
naturesQue MaxOss P Anorganic Bone Mineral EUDAMED
naturesQue MaxOss P GUDID
Generic name
Dental bone void filling material, animal-derived
Model / reference
58491
Primary DI / UDI-DI
00813954023458
Basic UDI-DI
B-00813954023458
FDA product code
NPM
EMDN code
Q010302 Dental graft devices
GMDN term
Dental bone void filling material, animal-derived
Device class
Class III EUDAMED
Class II GUDID
Regulation number
872.3930
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class III
GUDID
Class II

Device class is stated on each registry's own scale: Class III 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

Category: Dental bone matrix implant, animal-derived

Similar devices in this category

Other devices filed under DENTAL GRAFT DEVICES.

Other devices from Collagen Matrix, Inc.

See all devices from Collagen Matrix, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Contains animal tissues or cells
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (16, all answered No)