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Clamp

by CILITA Ltd. 3 variants

Ref F-120S, M-082T, GF-908, F-123S, F-121S, F-122SModel Clamp

Clamp (F-120S) is a medical device (EU MDR Class I; EMDN category hemostatic forceps) made by CILITA Ltd., registered in EUDAMED on 6 Feb 2025 (Basic UDI-DI 468017344CILCLMPGV), 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 Number468017344CILCLMPGV Basic UDI-DI Date6 Feb 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Clamp
Model / reference
Clamp, F-120S, M-082T, GF-908, F-123S, F-121S, F-122S
Primary DI / UDI-DI
04610274500012, 04610274531641, 04610274531764, 04610274500043, 04610274500029, 04610274500036
Basic UDI-DI
468017344CILCLMPGV
EMDN code
L031306 Hemostatic forceps, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
RU-MF-000041168
Authorised representative
Arazy Group GmbH DE-AR-000007685

Similar devices in this category

Other devices filed under HEMOSTATIC FORCEPS, REUSABLE.

Other devices from CILITA Ltd.

See all devices from CILITA Ltd. →

Properties

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