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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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Remisol Advance — 3 UDI-DI variants, IVDR (NORMAND-INFO S.A.S.U)

MD Atlas
NORMAND-INFO S.A.S.U

Data from EUDAMED, last updated May 19, 2026

Remisol Advance

150995908RADVH4

3 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: NORMAND-INFO S.A.S.U

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 150995908RADVH4
Device name: Remisol Advance
Device model: Remisol Advance v.2.3
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Special device type: refdata.special-ivd-device-type.software
Version date: Mar 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: NORMAND-INFO S.A.S.U
SRN: FR-MF-000024059
Country: France
Email: WITS_RA@beckman.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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basicUdiUlid01G3DJBEC6EMEC4PAP68WA34T2

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

REMISOL Advance15099590802073
C7394215099590750473
REMISOL Advance v 2.313700962601874