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Aprikos

by Aprikos Medical AS 1,000+ variants

Part of a family of 35 devices: see the family page

Ref AM22-120-08

Aprikos (AM22-120-08) is a Class I device made by Aprikos Medical AS, registered in EUDAMED on 15 May 2026 (Basic UDI-DI 7073371FILENO24X3), 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 Number7073371FILENO24X3 Basic UDI-DI Date15 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Trade name
Aprikos
Aprikos Medical
Device name
LP-24_Genral_Surgery_Forceps
ENT Instruments
Model / reference
AM22-120-08
Primary DI / UDI-DI
07073371059710, 07073371092694
Basic UDI-DI
7073371FILENO24X3, 7073371FILE105LF
Direct marketing DI
07073371059710
07073371092694
EMDN code
L031399, L149099
Device class
Class I
EU registration type
Standard device
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
NO-MF-000044411

Similar devices in this category

Other devices filed under GENERAL SURGERY FORCEPS, REUSABLE.

Other devices from Aprikos Medical AS

See all devices from Aprikos Medical AS →

Properties

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