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English Pattern Tooth Extracting Forcep Fig. 13 (For Lower Premolars) Stainless Steel

by Surtex Instruments Ltd

Ref DS-250-13Model 50554459GRASPOTIR150301FX

Active European Union

CE MDR CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 8 Nov 2026. What this means

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number50554459GRASPOTHERSAZ Basic UDI-DI 05055445993757UDI-DIDate13 Mar 2026RegisteredStatusActive
European UnionCE/MDR Number50554459GRASPOTHERSAZ Basic UDI-DI 05055445993757UDI-DIDate13 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device name
Grasping Instruments
Dental extraction tooth forceps, reusable
Model / reference
DS-250-13, 50554459GRASPOTIR150301FX
Primary DI / UDI-DI
05055445993757
Basic UDI-DI
50554459GRASPOTHERSAZ, B-05055445993757
EMDN code
L150301 Dental extraction tooth forceps, reusable
Device class
Class I
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
GB-MF-000023183
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Surtex Instruments Ltd.

See all devices from Surtex Instruments Ltd. →

Properties

  • Sterilise before use
  • Reusable

Other properties (12)

  • Supplied sterile: No
  • Implantable: No
  • Contains latex: No
  • Reprocessed single-use device: No
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
  • Incorporates a substance derived from human blood or plasma: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Contains endocrine-disrupting substances: No
  • Administering medicine: No
  • Measuring function: No
  • Incorporates a medicinal substance: No