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Tubifix a 3 Latex Free

by Plastic Electromechanic Company Medical International

Ref 106000003-10LF

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 Number61924911PECMI000133 Basic UDI-DI 06192491100353UDI-DIDate13 Jan 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
Tubifix
Model / Reference
106000003-10LF
Primary DI / UDI-DI
06192491100353
Basic UDI-DI
61924911PECMI000133
EMDN Code
M0303010103 Elastic fixing bandages, non-adhesive, extensible in two directions
Device Class
Class I
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
TN-MF-000004630
Authorised representative
HYDREX INTERNATIONAL FR-AR-000002216

Other devices from Plastic Electromechanic Company Medical International

See all devices from Plastic Electromechanic Company Medical International →

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