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Premier Probes

by Premier Dental Products Company 12 variants

Ref 1003670

Premier Probes (1003670) is a Class I device made by Premier Dental Products Company, registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI B-00348783006438) and listed in FDA GUDID since 17 Mar 2026 (UDI-DI 00348783006438), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

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/MDD EUDAMED NumberB-00348783006438 Basic UDI-DI 00348783006438UDI-DIDate30 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00348783006438 UDI-DI Date17 Mar 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00348783006438 registered 30 Sep 2026 Active
  • FDA GUDID UDI-DI 00348783006438 listed 17 Mar 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00348783006438
  2. Registered EUDAMED B-00348783006438

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic name
Dental surgical probe, reusable
Model / reference
1003670
Primary DI / UDI-DI
00348783006438
Basic UDI-DI
B-00348783006438
FDA product code
EIX
EMDN code
L159003 Dental and periodontal probes and explorers, reusable
GMDN term
Dental surgical probe, reusable
Device class
Class I
Regulation number
872.4565
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
US-MF-000015778
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under DENTAL AND PERIODONTAL PROBES AND EXPLORERS, REUSABLE.

Other devices from Premier Dental Products Company

See all devices from Premier Dental Products Company →

Properties

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