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Jota C254.HP.012

by Jota AG

Ref 500104415296012Model Rotary Instruments

Jota C254.HP.012 is a carbide dental bur (EU MDD Class IIa; FDA Class I; FDA product code GFF, Bur, Surgical, General & Plastic Surgery) made by Jota AG, registered in EUDAMED on 26 Jun 2026 (Basic UDI-DI B-EJOT500104415296012) and listed in FDA GUDID since 25 Jun 2025 (UDI-DI EJOT500104415296012), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-EJOT500104415296012 Basic UDI-DI EJOT500104415296012UDI-DIDate26 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEJOT500104415296012 UDI-DI Date25 Jun 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-EJOT500104415296012 registered 26 Jun 2026 Active
  • FDA GUDID UDI-DI EJOT500104415296012 listed 25 Jun 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID EJOT500104415296012
  2. Registered EUDAMED B-EJOT500104415296012

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  • Withdrawn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
Carbide dental bur, reusable
Model / reference
Rotary Instruments EUDAMED
500104415296012 EUDAMED
C254.HP.012 GUDID
Primary DI / UDI-DI
EJOT500104415296012
Basic UDI-DI
B-EJOT500104415296012
FDA product code
GFF
EMDN code
Q010399 Surgical dental devices - other
GMDN term
Carbide dental bur, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
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
500104415296012
GUDID
C254.HP.012
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.

Related devices

Category: Carbide dental bur, reusable

Similar devices in this category

Other devices filed under SURGICAL DENTAL DEVICES - OTHER.

Other devices from Jota AG

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)