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Wahoo II

by Professional Products, Inc. 2 variants

Ref 73238-08-01

Wahoo II (73238-08-01) is a Class I device made by Professional Products, Inc., registered in EUDAMED on 25 Mar 2026 (Basic UDI-DI 088369173238GE), withdrawn as of 24 Oct 2026.

Withdrawn Withdrawn in European Union.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

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number088369173238GE Basic UDI-DI 08836913051790UDI-DIDate25 Mar 2026RegisteredStatusWithdrawn No longer placed on the EU market

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device name
Wahoo II
Model / reference
73238-08-01
Primary DI / UDI-DI
08836913051790
Basic UDI-DI
088369173238GE
EMDN code
Y060603 Fingers orthoses
Device class
Class I
EU registration type
Standard device

Manufacturer details

EUDAMED SRN
US-MF-000019828
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Professional Products, Inc.

See all devices from Professional Products, Inc. →

Properties

Other properties (14, all answered No)