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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Gant d'examen en latex non poudrés,… — 5 UDI-DI variants, MDR

MD Atlas
CA Diffusion

Data from EUDAMED, last updated May 19, 2026

Gant d'examen en latex non poudrés, non stériles

376006117GANTLATEXNPQK

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: CA Diffusion

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376006117GANTLATEXNPQK
Device name: Gant d'examen en latex non poudrés, non stériles
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: CA Diffusion
SRN: FR-MF-000012222
Country: France
Email: info@cadiffusion.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K9782NGSV09BRRS9TW8JKHPK

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Gant Latex Non Poudre Large 8/9 - Boite x10003760061170100
Gant Latex Non Poudre Medium 7/8 - Boite x10003760061170094
Gant Latex Non Poudre Small 6/7 - Boite x10003760061170087
Gant Latex Non Poudre XLarge 9/10 - Boite x10003760061170117
Gant Latex Non Poudre XSmall 5/6 - Boite x10003760061171213