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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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HBPM Cuff — 4 UDI-DI variants, MDR (IEM GmbH)

MD Atlas
IEM GmbH

Data from EUDAMED, last updated May 23, 2026

HBPM Cuff

40413461009536

4 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: 40413461009536
Device name: HBPM Cuff
Device model: HBPM 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01KS05QD2NZP33NS00R116RSED

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

0404134610122404041346101224
0404134610121704041346101217
0404134610120004041346101200
0404134610123104041346101231