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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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Milieu RPMI 1640 — 5 UDI-DI variants, IVDR (Eurobio Scientific)

MD Atlas
Eurobio Scientific

Data from EUDAMED, last updated May 19, 2026

Milieu RPMI 1640

3661605CM1RPMNJ

5 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Eurobio Scientific

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 3661605CM1RPMNJ
Device name: Milieu RPMI 1640
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Oct 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: Eurobio Scientific
SRN: FR-MF-000011745
Country: France
Email: reglementaire@eurobio-scientific.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GF0Y75F6VKHY5HTGRW860QY4

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

RPMI 1640 media03366160500468
RPMI 1640 Media03366160500444
RPMI 1640 Media03366160500420
RPMI 1640 Media03366160500475
RPMI 1640 Media03366160500437