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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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Multichem AMH — 10 UDI-DI variants, IVDR

MD Atlas
Techno-path Manufacturing Ltd.

Data from EUDAMED, last updated May 24, 2026

Multichem AMH

539152344IMMA069L

10 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: Techno-path Manufacturing Ltd.

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Device characteristics

Professional testingHuman tissues / cells

Identity & classification

Basic UDI-DI: 539152344IMMA069L
Device name: Multichem AMH
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: May 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: Techno-path Manufacturing Ltd.
SRN: IE-MF-000001822
Country: Ireland
Email: bernd.hass@technopathcd.com
Phone: +353 61 525700

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQJ6021AMPAJB3THFWN82TE6

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

Multichem AMH05391523441353
Multichem AMH05391523441209
Multichem AMH05391523441360
Multichem AMH05391523441346
Multichem AMH05391523441377
Multichem AMH05391523441339
Multichem AMH05391523441193
Multichem AMH05391523441384
Multichem AMH05391523441315
Multichem AMH05391523441322