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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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FITC-labelled anti-human IgA — 2 UDI-DI variants, IVDR

MD Atlas
EUROIMMUN Medizinische Labordiagnostika AG

Data from EUDAMED, last updated May 23, 2026

FITC-labelled anti-human IgA

4049016AF101R85

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: EUROIMMUN Medizinische Labordiagnostika AG

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 4049016AF101R85
Device name: FITC-labelled anti-human IgA
Device model: AF 101-R
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: EUROIMMUN Medizinische Labordiagnostika AG
SRN: DE-MF-000005296
Country: Germany
Email: info@euroimmun.de
Phone: +49 451 2032-0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KHWV1QHQFXD3C6FDCMEHD1AG

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

FITC-labelled anti-human IgA04049016151593
FITC-labelled anti-human IgA04049016151227