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Clump holding forcep

by Prilanta Surgical

Ref 21100

Clump holding forcep (21100) is a Class I device made by Prilanta Surgical, registered in EUDAMED on 25 Jul 2024 (Basic UDI-DI ++G54821100K3), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G54821100K3 Basic UDI-DI G54821100-UDI-DIDate25 Jul 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
21100
Primary DI / UDI-DI
G54821100-
Basic UDI-DI
++G54821100K3
EMDN code
L03130402 Forceps for external bodies, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
PK-MF-000038228
Authorised representative
ANTEX MEDI SOLUTION DE-AR-000008078

Related devices

Category: Bronchoscopic biopsy curette, rigid

Similar devices in this category

Other devices filed under FORCEPS FOR EXTERNAL BODIES, REUSABLE.

Other devices from Prilanta Surgical

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Properties

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