Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

immuClone® (2) Anti-C IgM and Galileo — 5 UDI-DI variants, IVDR

MD Atlas
IMMUCOR Medizinische Diagnostik GmbH

Data from EUDAMED, last updated May 23, 2026

immuClone® (2) Anti-C IgM and Galileo

88823405W0103030202D27JM

5 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class D
Manufacturer: IMMUCOR Medizinische Diagnostik GmbH

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

ReagentProfessional testingHuman tissues / cellsAnimal tissues / cells

Legacy certificates

Certificate number: IX 1191616-4
Type: refdata.certificate-ivdr-type.technical-documentation
Notified body: TÜV Rheinland LGA Products GmbH (0197)
Validity: Dec 6, 2023 → Dec 5, 2028

Identity & classification

Basic UDI-DI: 88823405W0103030202D27JM
Device name: immuClone® (2) Anti-C IgM and Galileo
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class D
Version date: Dec 8, 2023

Manufacturer & authorised representative

Manufacturer

Name: IMMUCOR Medizinische Diagnostik GmbH
SRN: DE-MF-000006494
Country: Germany
Email: germany@immucor.com
Phone: +49 6103 8056 0

Variants by status

UDI-DI variants

5 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01HH4HSFQ5B5SGZ46HZYKPJ7PX

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

006601210888234300939
000721710888234300328
000720710888234300281
000721510888234300342
000720510888234300304