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Dr. Frei / medtex

by Medtex Swiss Ltd

Ref M0202

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 Number3800232484664TD Basic UDI-DI Date25 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  • Withdrawn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

Trade Name
Dr. Frei / medtex
Dr. Frei
Device Name
Three-layer disposable medical mask
Three-layer disposable medical mask with ties
Model / Reference
M0202
Primary DI / UDI-DI
03800232484664, 03800232484718, 03800232484725
Basic UDI-DI
3800232484664TD, 3800232484718TB, 3800232484725T8
EMDN Code
T020604 Medical use face masks, type II and iir
Device Class
Class I
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
BG-MF-000023453

Other devices from Medtex Swiss Ltd

See all devices from Medtex Swiss Ltd →

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