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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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ManyFlow/ Monoflow — 7 UDI-DI variants, MDR (MEDEX)

MD Atlas
MEDEX

Data from EUDAMED, last updated May 19, 2026

ManyFlow/ Monoflow

37005504M0002YV

7 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: MEDEX

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Device characteristics

Administers medicineAnimal tissues / cells

Identity & classification

Basic UDI-DI: 37005504M0002YV
Device name: ManyFlow/ Monoflow
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 31, 2025

Manufacturer & authorised representative

Manufacturer

Name: MEDEX
SRN: FR-MF-000000414
Country: France
Email: md-vigilance@guerbet.com
Phone: +33472792050

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01K1GNN7B04VBVRY5MF89TXMKP

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

FSDMU24113700550401039
FSDMU21113700550401022
FSDMU23113700550401046
FSDSU23113700550401015
FSDSU21113700550401008
FSDSU10113700550400988
FSDSU11113700550400995