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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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Semi-automatic Analyzer — 2 UDI-DI variants, IVDR (Diagnostica Stago)

MD Atlas
Diagnostica Stago

Data from EUDAMED, last updated May 19, 2026

Semi-automatic Analyzer

3607450INST0006UP

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: Diagnostica Stago

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 3607450INST0006UP
Device name: Semi-automatic Analyzer
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Nov 17, 2022

Manufacturer & authorised representative

Manufacturer

Name: Diagnostica Stago
SRN: FR-MF-000017089
Country: France
Email: webmaster@stago.com
Phone: +33 (0)1 46 88 20 20

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GJ2WA5587MNBHGG5HE122V51

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

5904103607450590418
5901703607450590173