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Jota 9501M.RA.030

by Jota AG

Ref 653204243513030Model Rotary Instruments

Jota 9501M.RA.030 is a device classified as Class IIa in the EU and Class I in the US made by Jota AG, registered in EUDAMED on 26 Jun 2026 (Basic UDI-DI B-EJOT653204243513030) and listed in FDA GUDID since 26 Sep 2023 (UDI-DI EJOT653204243513030), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-EJOT653204243513030 Basic UDI-DI EJOT653204243513030UDI-DIDate26 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEJOT653204243513030 UDI-DI Date26 Sep 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-EJOT653204243513030 registered 26 Jun 2026 Active
  • FDA GUDID UDI-DI EJOT653204243513030 listed 26 Sep 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID EJOT653204243513030
  2. Registered EUDAMED B-EJOT653204243513030

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  • Withdrawn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

Trade name
Jota
Generic name
Dental polishing brush
Model / reference
Rotary Instruments EUDAMED
653204243513030 EUDAMED
9501M.RA.030 GUDID
Primary DI / UDI-DI
EJOT653204243513030
Basic UDI-DI
B-EJOT653204243513030
FDA product code
EJQ
EMDN code
Q0199 Odontology devices - other
GMDN term
Dental polishing brush
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.6010
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

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
Rotary Instruments
653204243513030
GUDID
9501M.RA.030
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Similar devices in this category

Other devices filed under ODONTOLOGY DEVICES - OTHER.

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Properties

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