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Berten Extracting Forceps Fig.36, lower premolars

by GB Medical Instruments EUDAMED

Active European Union

Ref 87217

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-+G282ORIA1220O Basic UDI-DIDate20 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
87217
Primary DI / UDI-DI
+G282ORIA1220O
Basic UDI-DI
B-+G282ORIA1220O
EMDN Code
L150301 Dental extraction tooth forceps, reusable
Device Class
Class I
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
PK-MF-000009897
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from GB Medical Instruments

See all devices from GB Medical Instruments →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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