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Aprikos

by Aprikos Medical AS EUDAMED

Active European Union

Ref AM04-237-13

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7073371FILENO25X5 Basic UDI-DIDate15 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
LP-29 Hemostatic Forceps
Model / Reference
AM04-237-13
Primary DI / UDI-DI
07073371015570
Basic UDI-DI
7073371FILENO25X5
Direct Marketing DI
07073371015570
EMDN Code
L031306 Hemostatic forceps, reusable
Device Class
Class I
Market of Registration
Norway

Manufacturer details

EUDAMED SRN
NO-MF-000044411

Other devices from Aprikos Medical AS

See all devices from Aprikos Medical AS →

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