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Traumacel TAF Light

by BIOSTER, a.s. EUDAMED

Active European Union

Ref 60023

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number85903170010SG Basic UDI-DIDate7 May 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 24 0146 TD/NB Active

    Technical documentation EU MDR

    Notified body
    1023
    Issued
    29 Apr 2024
    Expires
    28 Apr 2029

Specification

EUDAMED

Device Name
Traumastem
Model / Reference
60023
Primary DI / UDI-DI
18590317600233
Basic UDI-DI
85903170010SG
EMDN Code
M040501 Polysaccharide haemostatic dressings
Device Class
Class III
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000011615

Other devices from BIOSTER, a.s.

See all devices from BIOSTER, a.s. →

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