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Aprikos

by Aprikos Medical AS Norway EUDAMED

Ref AM04-220-16

EMDN L031306

Regulatory status

as of 24 Oct 2026

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

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
LP-29 Hemostatic Forceps
Model / Reference
AM04-220-16
Primary DI / UDI-DI
07073371015389
Basic UDI-DI
7073371FILENO25X5
Direct Marketing DI
07073371015389
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 & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 66cb8ea0-37df-4073-b1e3-c3ea182d42f4 61 fields · synced 23 Oct 2026