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MediTrac

by Flex-Trac, Inc. 31 variants

Ref MTSI-1500-SFModel MEDITRAC CMT

Active European Union

CE MDR

Valid until

3 Sep 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

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 Number0850076450MTSIZM Basic UDI-DIDate23 Sep 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • US26/00000389 Active

    Quality management system EU MDR

    Notified body
    SGS Belgium NV 1639
    Issued
    3 Sep 2026
    Expires
    3 Sep 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
MEDITRAC CMT, MTSI-1500-SF
Primary DI / UDI-DI
00850076450168
Basic UDI-DI
0850076450MTSIZM
EMDN Code
Z120309 Medical/medicinal gas pipeline systems and related accessories
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
US-MF-000050962
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Flex-Trac, Inc.

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See all devices from Flex-Trac, Inc. →

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