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Gant Vinyle Poudre Naturel T.xl C/10BTE Distri X 100

by SARL Mutexil

Ref 6661210-XL

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 25 Oct 2026. What this means

Overview

This medical device, GANT VINYLE POUDRE NATUREL T.XL C/10BTE DISTRI X 100, is a Class I medical device manufactured by SARL MUTEXIL. It is used for the treatment of various medical conditions and is approved under regulatory ID -197. The device has undergone professional testing, with its version number being 1. The device is not reusable and does not have any specific legal or legislative applications. Its classification as a Class I device indicates that it meets certain safety and performance standards.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37011023GANTBY Basic UDI-DI 03701102300308UDI-DIDate10 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  • Withdrawn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
Gant
Model / Reference
6661210-XL
Primary DI / UDI-DI
03701102300308
Basic UDI-DI
37011023GANTBY
Unit of Use DI
03701102300315
EMDN Code
T01020201 Vinyl examination / treatment gloves
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000045229

Other devices from SARL Mutexil

See all devices from SARL Mutexil →

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