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Biofill Kanüle

by Human Med AG

Ref 580086

Biofill Kanüle (580086) is a Class IIa device made by Human Med AG, registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI B-04260170881243), 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-04260170881243 Basic UDI-DI 04260170881243UDI-DIDate2 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
WAL cannula
Model / reference
580086
Primary DI / UDI-DI
04260170881243
Basic UDI-DI
B-04260170881243
EMDN code
L030101 Suction and irrigation surgical cannulas and handpieces, reusable
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000013901

Similar devices in this category

Other devices filed under SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLE.

Other devices from Human Med AG

See all devices from Human Med AG →

Properties

  • Sterilise before use
  • Reusable
Other properties (10, all answered No)