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Arm Sling

by Welsheng Corp. 4 variants

Ref 839-BL-XL-1

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471988489CL101GG Basic UDI-DI 04719890062376UDI-DIDate7 Sep 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  • Withdrawn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
Immobilisation Bandages
Model / Reference
839-BL-XL-1
Primary DI / UDI-DI
04719890062376
Basic UDI-DI
471988489CL101GG
EMDN Code
M030501 Immobilisation bandages for shoulder, arm and collarbone
Device Class
Class I
EU market of registration
Malta

Manufacturer details

EUDAMED SRN
TW-MF-000005197
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Other devices from Welsheng Corp.

See all devices from Welsheng Corp. →

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