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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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KALIN — 10 UDI-DI variants, MDR (WINNCARE FRANCE)

MD Atlas
WINNCARE FRANCE

Data from EUDAMED, last updated May 19, 2026

KALIN

366489702194HZ

10 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: 366489702194HZ
Device name: KALIN
Device model: KALIN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ8754SNZC0YVYSQ7FSANW6H

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

PO3P4D03664897023145
PO3P4D1503664897025323
PO3P4D0603664897023473
PO3P4D0403664897023466
PO3P4D1403664897023480
PO3P4AD03664897023428
PO3P4AD0303664897023435
PO3P4D0303664897023459
PO3P4ABD03664897023411
PO3P4BD03664897023442