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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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ABPM Cuff — 9 UDI-DI variants, MDR (IEM GmbH)

MD Atlas
IEM GmbH

Data from EUDAMED, last updated May 23, 2026

ABPM Cuff

40413461009332

9 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: IEM GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40413461009332
Device name: ABPM Cuff
Device model: ABPM cuff
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: IEM GmbH
SRN: DE-MF-000005735
Country: Germany
Email: regulatory@iem.de

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KRZVNBVHEBD45X0562G8YVX2

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

0404134610105704041346101057
0404134610213904041346102139
0404134610212204041346102122
0404134610104004041346101040
0404134610211504041346102115
0404134610106404041346101064
0404134610214604041346102146
0404134610102604041346101026
0404134610210804041346102108