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Retaining Screw for Digital Model Analog

by Adin Dental Implant Systems LTD.

Ref RS1002Model Analog

Retaining Screw for Digital Model Analog (RS1002) is a Class I device made by Adin Dental Implant Systems Ltd., registered in EUDAMED on 12 Mar 2024 (Basic UDI-DI 729010930DigitAnalogRepCV) and listed in FDA GUDID since 2 May 2021 (UDI-DI 07290109301877), 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 Number729010930DigitAnalogRepCV Basic UDI-DI 07290109301877UDI-DIDate12 Mar 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number07290109301877 UDI-DI Date2 May 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 729010930DigitAnalogRepCV registered 12 Mar 2024 Active
  • FDA GUDID UDI-DI 07290109301877 listed 2 May 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07290109301877
  2. Registered EUDAMED 729010930DigitAnalogRepCV

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  • Withdrawn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
Dental prosthesis/implant abutment screw
Model / reference
Analog, RS1002
Primary DI / UDI-DI
07290109301877
Basic UDI-DI
729010930DigitAnalogRepCV
FDA product code
NDP
EMDN code
Q010207 Dental impression devices for prosthetic dentistry
GMDN term
Dental prosthesis/implant abutment screw
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

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Sterilise before useEUDAMED
No
GUDID
Yes
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 07290109301877: EUDAMED states No, FDA GUDID states Yes.

Manufacturer details

EUDAMED SRN
IL-MF-000014625
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Related devices

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

Similar devices in this category

Other devices filed under DEVICES FOR PROSTHETIC DENTISTRY.

Other devices from Adin Dental Implant Systems Ltd.

See all devices from Adin Dental Implant Systems Ltd. →

Properties

  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (18, all answered No)