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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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Mueller Hinton Broth — 1 UDI-DI variant, IVDR (Fannin Ltd.)

MD Atlas
Fannin Ltd.

Data from EUDAMED, last updated May 30, 2026

Mueller Hinton Broth

53915118586413E

1 UDI-DI variant

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: Fannin Ltd.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 53915118586413E
Device name: Mueller Hinton Broth
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Fannin Ltd.
SRN: IE-MF-000002373
Country: Ireland
Email: Quality@fannin.eu
Phone: +35312907000

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSQJ8E9536QKVTGN6X35NS09

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

W1403405391511832767