Skip to content

Extraction cannula, 300 mm

by Human Med AG

Ref 655010

Extraction cannula, 300 mm (655010) is a Class IIa device made by Human Med AG, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-14260170881424), withdrawn as of 7 Nov 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

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-14260170881424 Basic UDI-DI 14260170881424UDI-DIDate5 Nov 2026RegisteredStatusWithdrawn No longer placed on the EU market

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Withdrawn

Specification

EUDAMED

Device name
Extraction cannula
Model / reference
655010
Primary DI / UDI-DI
14260170881424
Basic UDI-DI
B-14260170881424
EMDN code
A0680 Drainage and fluid collection devices - accessories
Device class
Class IIa
EU registration type
Legacy device (under a directive)

Manufacturer details

EUDAMED SRN
DE-MF-000013901

Similar devices in this category

Other devices filed under DRAINAGE AND FLUID COLLECTION DEVICES - ACCESSORIES.

Other devices from Human Med AG

See all devices from Human Med AG →

Properties

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