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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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AXTAIR — 184 UDI-DI variants, MDR (WINNCARE FRANCE)

MD Atlas
WINNCARE FRANCE

Data from EUDAMED, last updated May 19, 2026

AXTAIR

366489700083H9

184 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: WINNCARE FRANCE

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Device characteristics

Active device

Clinical investigations

Registered: No

Legacy certificates

Certificate number: FR26/00000124
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: SGS Belgium NV (1639)
Validity: Apr 14, 2026 → Apr 14, 2031

Identity & classification

Basic UDI-DI: 366489700083H9
Device name: AXTAIR
Device model: AXTAIR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 4, 2025

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

184 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KBMHHM871APQ4AHQJ230GCMY

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

No registered UDI-DI variants for this device family.