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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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Lotion traitante Flash AROMAPOUX — 3 UDI-DI variants, MDR

MD Atlas
TAG LIFECARE

Data from EUDAMED, last updated May 19, 2026

Lotion traitante Flash AROMAPOUX

37014371BU684X10XCL1SS

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: TAG LIFECARE

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 37014371BU684X10XCL1SS
Device name: Lotion traitante Flash AROMAPOUX
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 12, 2024

Manufacturer & authorised representative

Manufacturer

Name: TAG LIFECARE
SRN: FR-MF-000000300
Country: France
Email: contact@taglifecare.com
Phone: +33254467837

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HV8THF431NQVFWS76V2R5164

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

BU684-1003701437100079
AROMAPOUX03701437100055
Lotion traitante Flash AROMAPOUX03701437100130