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Biofill Applikator

by Human Med AG

Ref 580001

Biofill Applikator (580001) is a Class IIa device made by Human Med AG, registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-14260170881158), 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-14260170881158 Basic UDI-DI 14260170881158UDI-DIDate3 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  • Withdrawn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 Applikator
Model / reference
580001
Primary DI / UDI-DI
14260170881158
Basic UDI-DI
B-14260170881158
EMDN code
Z120105 Surgical medical aspirators
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 SURGICAL MEDICAL ASPIRATORS.

Other devices from Human Med AG

See all devices from Human Med AG →

Properties

  • Supplied sterile
  • Administering medicine
Other properties (10, all answered No)