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Eztetic® NPTRAY

by ZimVie US Corp LLC

Part of a family of 7 devices: see the family page

Ref NPTRAY

Eztetic® NPTRAY is a Class I device made by ZimVie US Corp LLC, registered in EUDAMED on 27 May 2026 (Basic UDI-DI 844868A9HA) and listed in FDA GUDID since 18 Aug 2017 (UDI-DI 00889024343979), 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 Number844868A9HA Basic UDI-DI 00889024343979UDI-DIDate27 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024343979 UDI-DI Date18 Aug 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 844868A9HA registered 27 May 2026 Active
  • FDA GUDID UDI-DI 00889024343979 listed 18 Aug 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889024343979
  2. Registered EUDAMED 844868A9HA

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  • Withdrawn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
Eztetic®
Generic name
Dental implant/prosthesis surgical procedure kit
Device name
Dental Instrument Trays
Model / reference
NPTRAY
Primary DI / UDI-DI
00889024343979
Basic UDI-DI
844868A9HA
FDA product code
DZA
EMDN code
Q0199 Odontology devices - other
GMDN term
Dental implant/prosthesis surgical procedure kit
Device class
Class I
Regulation number
872.4130
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental implant/prosthesis surgical procedure kit

Similar devices in this category

Other devices filed under ODONTOLOGY DEVICES - OTHER.

Other devices from ZimVie US Corp LLC

See all devices from ZimVie US Corp LLC →

Properties

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