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LT150

by ZimVie US Corp LLC

Part of a family of 75 devices: see the family page

Ref LT150

LT150 is a Class I device made by ZimVie US Corp LLC, registered in EUDAMED on 3 Jun 2026 (Basic UDI-DI 844868A5H2) and listed in FDA GUDID since 18 Jan 2016 (UDI-DI 00844868009689), 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 Number844868A5H2 Basic UDI-DI 00844868009689UDI-DIDate3 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00844868009689 UDI-DI Date18 Jan 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 844868A5H2 registered 3 Jun 2026 Active
  • FDA GUDID UDI-DI 00844868009689 listed 18 Jan 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00844868009689
  2. Registered EUDAMED 844868A5H2

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  • Withdrawn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

Generic name
Surgical drill guide, reusable
Device name
Dental Laboratory Tools
Model / reference
LT150
Primary DI / UDI-DI
00844868009689
Basic UDI-DI
844868A5H2
FDA product code
NDP
EMDN code
Q0199 Odontology devices - other
GMDN term
Surgical drill guide, reusable
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Sterilise before useEUDAMED
Yes
GUDID
No

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 00844868009689: EUDAMED states Yes, FDA GUDID states No.

Related devices

Category: Surgical drill guide, reusable

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 YesEUDAMEDNoGUDID
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)