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Stretcher

by ZJG Royaltrust Med CO., LTD 28 variants

Ref RC-C5Model RC-A1,RC-A2,RC-A3,RC-A4,RC-A5,RC-A6,RC-A7, RC-B1,RC-B2,RC-B3,RC-B4,RC-B5,RC-B6, RC-C1,RC-C2,RC-C3,RC-C4,RC-C5, RC-D1,RC-D2,RC-D3,RC-D4,RC-D5, RC-E1,RC-E1A,RC-E1S,RC-E2,RC-E2S,RC-E3,RC-E4,RC-E5,RC-E6,RC-E7,RC-E8,RC-E9 RC-F1,RC-F2,RC-F3,RC-F5, etc

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 Number697569672RC001QJ Basic UDI-DI 06975696720836UDI-DIDate26 Feb 2025RegisteredStatusActive

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  • Withdrawn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
Stretcher
Model / Reference
RC-A1, RC-A2, RC-A3, RC-A4, RC-A5, RC-A6, RC-A7, RC-B1, RC-B2, RC-B3, RC-B4, RC-B5, RC-B6, RC-C1, RC-C2, RC-C3, RC-C4, RC-C5, RC-D1, RC-D2, RC-D3, RC-D4, RC-D5, RC-E1, RC-E1A, RC-E1S, RC-E2, RC-E2S, RC-E3, RC-E4, RC-E5, RC-E6, RC-E7, RC-E8, RC-E9 RC-F1, RC-F2, RC-F3, RC-F5, etc
Primary DI / UDI-DI
06975696720836
Basic UDI-DI
697569672RC001QJ
EMDN Code
V08050199 Patient transfer stretchers - other
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000029362
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from ZJG Royaltrust Med CO., LTD

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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