Skip to content

ArtiAid

by Maxigen Biotech Inc.

Ref AA-25

ArtiAid (AA-25) is a Class III device made by Maxigen Biotech, Inc., registered in EUDAMED on 26 May 2026 (Basic UDI-DI B-04714691810195), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04714691810195 Basic UDI-DI Date26 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
ArtiAid Intra-articular Injection
Model / reference
AA-25
Primary DI / UDI-DI
04714691810195, 04714691810201, 04714691810188
Basic UDI-DI
B-04714691810195, B-04714691810201, B-04714691810188
EMDN code
P900402 Resorbable filling and reconstruction devices
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
Poland
Spain

Manufacturer details

EUDAMED SRN
TW-MF-000010390
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Similar devices in this category

Other devices filed under RESORBABLE FILLING AND RECONSTRUCTION DEVICES.

Other devices from Maxigen Biotech, Inc.

See all devices from Maxigen Biotech, Inc. →

Properties

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