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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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DUO DIVISYS — 68 UDI-DI variants, MDR (WINNCARE FRANCE)

MD Atlas
WINNCARE FRANCE

Data from EUDAMED, last updated May 19, 2026

DUO DIVISYS

366489700501H6

68 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: WINNCARE FRANCE

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 366489700501H6
Device name: DUO DIVISYS
Device model: DUO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: WINNCARE FRANCE
SRN: FR-MF-000000482
Country: France
Email: contact@winncare.fr
Phone: +33 4 66 02 15 15

Variants by status

UDI-DI variants

68 UDI-DI variants

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Applied filters

basicUdiUlid01KPVECXFTEFQS7C5YKAVZJHA4

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

DO8P8A1CI03664897010398
DO8P9A1CS03664897010688
DO8P8I0603664897010541
DO8P9CI03664897010824
DO8P8I03664897010534
DO8C9A103664897010268
DO8P8A1I03664897010404
DO8C9A303664897010305
DO8P9A1S0303664897023350
DO8P9A3C03664897010763
DO8P9A10303664897028386
DO8P8CS03664897032123
DO8P9A303664897000313
DO8P80303664897010350
DO8P8A3C03664897010466
DO8P9A1S03664897010718
DO8P8A1CS03664897023794
DO8P803664897010343

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