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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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Pack FLUXMED — 10 UDI-DI variants, MDR (MDB TEXINOV)

MD Atlas
MDB TEXINOV

Data from EUDAMED, last updated May 19, 2026

Pack FLUXMED

3770021816FLUXMEDJ8

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: MDB TEXINOV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770021816FLUXMEDJ8
Device name: Pack FLUXMED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: MDB TEXINOV
SRN: FR-MF-000001728
Country: France
Email: moudot@texinov.fr
Phone: +33 437050523

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KEVZAX8HATEEPTXG0JMZFP5G

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

FLUXMED 1V103770021816139
FLUXMED 1V203770021816085
FLUXMED 2V103770021816122
FLUXMED 2V203770021816078
FLUXMED 3V103770021816115
FLUXMED 3V203770021816061
FLUXMED 4V103770021816108
FLUXMED 4V203770021816054
FLUXMED 6V103770021816092
FLUXMED 6V203770021816047