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TRAUMA BANDAGE 20cm

by Ivf Hartmann AG 4 variants

Ref 831375Model 3207

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 linked in EUDAMED

A group certificate may exist

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 Number76116003207MC Basic UDI-DI 07611600994731UDI-DIDate23 Jan 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Trauma Bandage
Model / Reference
3207, 831375
Primary DI / UDI-DI
07611600994731
Basic UDI-DI
76116003207MC
EMDN Code
M0304010103 Elastic compression bandages, non-adhesive, high extensibility (>140%)
Device Class
Class I
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
CH-MF-000015962
Authorised representative
PAUL HARTMANN AG DE-AR-000007519

Other devices from Ivf Hartmann AG

See all devices from Ivf Hartmann AG →

Properties

  • Sterile

Other properties (12)

  • 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