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Kinder Dl

by Biopsybell SRL 13 variants

Ref 12KKN2V-Y

Kinder Dl (12KKN2V-Y) is a Class IIa device made by Biopsybell SRL, registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-08033860030506), active as of 7 Nov 2026.

Active European Union

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08033860030506 Basic UDI-DI 08033860030506UDI-DIDate3 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
12KKN2V-Y
Primary DI / UDI-DI
08033860030506
Basic UDI-DI
B-08033860030506
EMDN code
U08020202 Double lumen needles and sets/systems for oocyte retrieval
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000011601

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Other devices filed under DEVICES FOR ASSISTED REPRODUCTION.

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Properties

  • Supplied sterile
Other properties (11, all answered No)