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Neodent 108.172

by JJGC Indústria e Comércio de Materiais Dentários S/A.

Part of a family of 10 devices: see the family page

Ref 108.172Model Abutment

Neodent 108.172 is a Class I device made by JJGC Indústria e Comércio de Materiais Dentários S/A., registered in EUDAMED on 6 May 2026 (Basic UDI-DI 987800090VS) and listed in FDA GUDID since 12 Dec 2022 (UDI-DI 07899878026747), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number987800090VS Basic UDI-DI 07899878026747UDI-DIDate6 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07899878026747 UDI-DI Date12 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 987800090VS registered 6 May 2026 Active
  • FDA GUDID UDI-DI 07899878026747 listed 12 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07899878026747
  2. Registered EUDAMED 987800090VS

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  • Withdrawn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
Neodent
Generic name
Dental implant suprastructure, temporary, preformed, single-use
Device name
Abutment Impression Copings
Model / Ref / Catalog
108.172, Abutment
Primary DI / UDI-DI
07899878026747
Basic UDI-DI
987800090VS
FDA product code
NDP
EMDN code
Q010599 Dental instruments, single-use - other
GMDN term
Dental implant suprastructure, temporary, preformed, single-use
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Length — 4 Millimeter
Outer Diameter — 3.3 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Sterilise before useEUDAMED
Yes
GUDID
No
ImplantableEUDAMED
No
GUDID
Yes

Registry differences

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

  • Sterilise before use UDI-DI 07899878026747: EUDAMED states Yes, FDA GUDID states No.

Related devices

Category: Dental implant suprastructure, temporary, preformed, single-use

Similar devices in this category

Other devices filed under DENTAL INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from JJGC Indústria e Comércio de Materiais Dentários S/A.

See all devices from JJGC Indústria e Comércio de Materiais Dentários S/A. →

Properties

  • Supplied sterile
  • Sterilise before use YesEUDAMEDNoGUDID
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (16, all answered No)