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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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POSIMO — 8 UDI-DI variants, MDR (WINNCARE FRANCE)

MD Atlas
WINNCARE FRANCE

Data from EUDAMED, last updated May 19, 2026

POSIMO

366489700099HQ

8 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 366489700099HQ
Device name: POSIMO
Device model: VPOS
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

8 UDI-DI variants

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Applied filters

basicUdiUlid01KPVDGVH8WCVFMPGX49JQJR2W

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

Heel support POSIMO03664897004885
VTLA/HIPH03664897004908
VTM/5403664897004922
VCDA/5003664897002508
VTAC450/CIC03664897004892
VDT41A/CIC03664897002720
VDT45A/CIC03664897002737
VTLAXL/HIPH03664897004915