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Surgimax

by Surgimax Instruments Ltd 13 variants

Ref 05-130-01Model 0426DF

Active European Union

CE MDR

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/MDR Number5060520350426DF7Q Basic UDI-DI 05060520352510UDI-DIDate24 Aug 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Forceps
Model / Reference
0426DF, 05-130-01
Primary DI / UDI-DI
05060520352510
Basic UDI-DI
5060520350426DF7Q
Direct Marketing DI
05060520352510
EMDN Code
L03130403 Splinter forceps, reusable
Device Class
Class I
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
UK-MF-000042610
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Surgimax Instruments Ltd

See all devices from Surgimax Instruments Ltd →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No