Skip to content

Emergency Blanket

by FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU) 8 variants

Ref FS-136G

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 Number69422726P3.03.01XA Basic UDI-DI 16942272651362UDI-DIDate11 May 2022RegisteredStatusActive

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  • Withdrawn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
FS-136G
Primary DI / UDI-DI
16942272651362
Basic UDI-DI
69422726P3.03.01XA
Unit of Use DI
06942272651365
EMDN Code
Y090699 Devices for body protection - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000009645
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU)

See all devices from FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU) →

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