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Traverse Rescue Stretcher

by Traverse Rescue LLC 2 variants

Ref 19-0100AModel Traverse Rescue 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number83156600V08050101TRSUV Basic UDI-DI 00831566001053UDI-DIDate20 Jul 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
Traverse Rescue Stretcher, 19-0100A
Primary DI / UDI-DI
00831566001053
Basic UDI-DI
83156600V08050101TRSUV
Direct Marketing DI
00831566001053
EMDN Code
V08050101 Generic use stretchers
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CA-MF-000037070
Authorised representative
Ferno S.r.l. IT-AR-000031265

Other devices from Traverse Rescue LLC

See all devices from Traverse Rescue LLC →

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