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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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WIN-POD — 3 UDI-DI variants, MDR (Medicapteurs France)

MD Atlas
Medicapteurs France

Data from EUDAMED, last updated May 19, 2026

WIN-POD

377003277Winpod99

3 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: Medicapteurs France

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 377003277Winpod99
Device name: WIN-POD
Device model: WINPOD v4
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: Medicapteurs France
SRN: FR-MF-000027379
Country: France
Email: info@medicapteurs.fr
Phone: +33 5 571 571

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HYMXXA06NJH4ADZTZ5DBVDH8

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

WIN-POD Blanche03770032770024
WIN-POD Noire03770032770017
WINPOD GEBIOM GO-TEC03770032770345