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Pinzette

by Geister Medizintechnik GmbH 1,000+ variants

Part of a family of 1,281 devices: see the family page

Ref 10-3561.DF

Pinzette (10-3561.DF) is a Class I device made by Geister Medizintechnik GmbH, registered in EUDAMED on 9 Oct 2026 (Basic UDI-DI 4057034000000092A), active as of 22 Oct 2026.

Active European Union

CE MDR

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4057034000000092A Basic UDI-DI 04057034025888UDI-DIDate9 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Pinzette
Model / reference
10-3561.DF
Primary DI / UDI-DI
04057034025888
Basic UDI-DI
4057034000000092A
Direct marketing DI
04057034025888
EMDN code
L031308 Surgical and anatomical tweezers, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005461

Similar devices in this category

Other devices filed under SURGICAL AND ANATOMICAL TWEEZERS, REUSABLE.

Other devices from Geister Medizintechnik GmbH

See all devices from Geister Medizintechnik GmbH →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)