Oasis

Device Name

Oasis

Model / Reference

OASIS-PC

Primary DI / UDI-DI

00628774362003

Basic UDI-DI

62877436200UR

Direct Marketing DI

00628774362003

EMDN Code

Y122127 Electric wheelchairs

Device Class

Class I

Market of Registration

France

EUDAMED SRN

CA-MF-000048427

Authorised representative

HOME MEDICAL SERVICE H.M.S. FR-AR-000047948

• Oasis

  Class I

  CE/MDR

• Karma-Rs, Karma-Fs Wheelchairs

  Class II

  FDA 510(k) K884812 Active Cleared 27 Dec 1988

• Powered Wheelchair

  Class II

  FDA 510(k) K962565 Active Cleared 20 Mar 1997

• Apollo Sterile Blades

  Class I

  FDA 510(k) K852661 Active Cleared 11 Jul 1985

• Orthofab Wheelchair Astra (Folding Manual Wheelchair)

  Class I

  FDA 510(k) K950904 Active Cleared 5 Apr 1995

• Orthofab Wheelchair Ultima (Rigid Frame Manual Wheelchair)

  Class I

  FDA 510(k) K950903 Active Cleared 5 Apr 1995

See all devices from Orthofab inc. →