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ViVi® PULL-OVER TOGA SIZE XL-XXL

by THI Total Healthcare Innovation GmbH 2 variants

Ref 80230V

Active European Union

CE MDR

Valid until

14 Apr 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DQS Medizinprodukte GmbH

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 Number1000302998 Date19 Feb 2026IssuedStatusActive expires 14 Apr 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000302998 Active Supplemented

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    19 Feb 2026
    Expires
    14 Apr 2030
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
ViVi® GOWNS 80XXX
Model / Reference
80230V
Primary DI / UDI-DI
09009607812307
Basic UDI-DI
9009607GOWNS80XXXD4
EMDN Code
T020401 Standard surgical gowns
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
AT-MF-000044495

Other devices from Thi Total Healthcare Innovation GmbH

See all devices from Thi Total Healthcare Innovation GmbH →

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