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Bethel Tip 21G Long Straight

by Bethel Co., Ltd.

Ref X022P1910KModel Bethel Dental Tip

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number458000333DENTTIPAPPIRRVE Basic UDI-DI 04580003330244UDI-DIDate16 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Bethel Dental Application / Irrigation Tips
Model / Reference
Bethel Dental Tip, X022P1910K
Primary DI / UDI-DI
04580003330244
Basic UDI-DI
458000333DENTTIPAPPIRRVE
EMDN Code
Q010199 Conservative dentistry and endodontics devices - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
JP-MF-000054354
Authorised representative
Easy Medical Device CommV BE-AR-000011902

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No