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KEISEI Super Micro Forceps 14cm

by Keisei Medical Industrial Co., Ltd. 2 variants

Ref DNH-158R

Active European Union

CE MDD

Valid until

Not listed

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-34946279746126 Basic UDI-DI 34946279746126UDI-DIDate28 Apr 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  • Withdrawn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 Active

Specification

EUDAMED

Model / Reference
DNH-158R
Primary DI / UDI-DI
34946279746126
Basic UDI-DI
B-34946279746126
EMDN Code
L0205 Needle holders, reusable
Device Class
Class I
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
JP-MF-000021775
Authorised representative
mdi Europa GmbH DE-AR-000006218

Related devices

Category: Suturing needle holder, reusable

Other devices from Keisei Medical Industrial Co., Ltd.

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Properties

  • Sterile
  • Reusable

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No