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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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ENHANCEMENT MEDIA (E.G. BOVINE… — 2 UDI-DI variants, IVDR (DIAGAST)

MD Atlas
DIAGAST

Data from EUDAMED, last updated May 19, 2026

ENHANCEMENT MEDIA (E.G. BOVINE ALBUMIN,LISS,PEG)

3661562ALISSXXXXXXXXXXXXQ

2 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: DIAGAST

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 3661562ALISSXXXXXXXXXXXXQ
Device name: ENHANCEMENT MEDIA (E.G. BOVINE ALBUMIN,LISS,PEG)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: DIAGAST
SRN: FR-MF-000012310
Country: France
Email: contact@diagast.com
Phone: 33 (0)3 20 96 53 53

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ71T00G6YKEY1SKWTG0ZCMA

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

6901323661562690132
7302923661562730296