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Neodent 108.335

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

Part of a family of 35 devices: see the family page

Ref 108.235Model Instrument

Neodent 108.335 is a Class I device made by JJGC Indústria e Comércio de Materiais Dentários S/A., registered in EUDAMED on 8 May 2026 (Basic UDI-DI 987800095W4) and listed in FDA GUDID since 19 Nov 2024 (UDI-DI 07899878061113), 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 Number987800095W4 Basic UDI-DI 07899878061113UDI-DIDate8 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07899878061113 UDI-DI Date19 Nov 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 987800095W4 registered 8 May 2026 Active
  • FDA GUDID UDI-DI 07899878061113 listed 19 Nov 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07899878061113
  2. Registered EUDAMED 987800095W4

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  • Withdrawn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, reusable
Device name
Reusable Implant Impression Copings
Model / Ref / Catalog
Instrument EUDAMED
108.235 EUDAMED
108.335 GUDID
Primary DI / UDI-DI
07899878061113
Basic UDI-DI
987800095W4
FDA product code
NDP
EMDN code
Q0199 Odontology devices - other
GMDN term
Dental implant suprastructure, temporary, preformed, reusable
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Height — 2.5 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
Instrument
108.235
GUDID
108.335
ImplantableEUDAMED
No
GUDID
Yes

Related devices

Category: Dental implant suprastructure, temporary, preformed, reusable

Similar devices in this category

Other devices filed under ODONTOLOGY DEVICES - 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

  • Sterilise before use
  • Implantable NoEUDAMEDYesGUDID
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (17, all answered No)