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Raven 90C Bi-Fold Stretcher

by Golden Season Pte Ltd

Ref RAVEN 90C BI-FOLD STRETCHER

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8885020558885020550153W4 Basic UDI-DI 08885020550153UDI-DIDate1 Nov 2023RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
Raven 90C Bi-Fold Stretcher
Model / Reference
RAVEN 90C BI-FOLD STRETCHER
Primary DI / UDI-DI
08885020550153
Basic UDI-DI
8885020558885020550153W4
EMDN Code
V08050101 Generic use stretchers
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
SG-MF-000031816
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Golden Season Pte Ltd

See all devices from Golden Season Pte Ltd →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No