Skip to content

Spartan Titanium 2pc Plastic Shell Rescue Litter

by Traverse Rescue LLC

Ref 11-0127TI

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 Number83156600V08050101SPTIAQ Basic UDI-DI 00831566000308UDI-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  • Withdrawn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

Device Name
Spartan Titanium 2pc Plastic Shell Rescue Litter
Model / Reference
11-0127TI
Primary DI / UDI-DI
00831566000308
Basic UDI-DI
83156600V08050101SPTIAQ
Direct Marketing DI
00831566000308
EMDN Code
V08050101 Generic use stretchers
Device Class
Class I
EU market of registration
Italy

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