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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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MUC2 G4 HAYDN BED — 4 UDI-DI variants, MDR (THUASNE)

MD Atlas
THUASNE

Data from EUDAMED, last updated May 19, 2026

MUC2 G4 HAYDN BED

311179FR0125AEW

4 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: THUASNE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 311179FR0125AEW
Device name: MUC2 G4 HAYDN BED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: THUASNE
SRN: FR-MF-000001201
Country: France
Email: service.conseil@thuasne.fr
Phone: +33 4 77 81 40 40

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JXZX23VMXM85BGC8M9Q4M1MT

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

V21492722203111792927226
V200654000103111792065416
V22491011003111792241100
V200754000103111792075415