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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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GELTOP — 5 UDI-DI variants, MDR (WINNCARE FRANCE)

MD Atlas
WINNCARE FRANCE

Data from EUDAMED, last updated May 19, 2026

GELTOP

366489700097HL

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: WINNCARE FRANCE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 366489700097HL
Device name: GELTOP
Device model: VAB
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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KPVBDQ6K16SPKVMM58AKESPC

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

VAB4345/PUHD03664897021899
VAB4345/CIC03664897021875
VAB40TH03664897001631
VAB4040/CIC03664897021868
VAB4040/PUHD03664897021882