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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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Cuff — 6 UDI-DI variants, MDR (SOMNOmedics AG)

MD Atlas
SOMNOmedics AG

Data from EUDAMED, last updated May 23, 2026

Cuff

42504134ABPM-ManCX

6 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: SOMNOmedics AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42504134ABPM-ManCX
Device name: —
Device model: Cuff
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: SOMNOmedics AG
SRN: DE-MF-000006921
Country: Germany
Email: qmra@somnomedics.de

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KPDR740BBS3H5E0E1C479TA1

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

ABP502R04250413406470
ABP500R04250413406456
ABP501R04250413406463
ABP501/B04250413403578
ABP500/B04250413403561
ABP502/B04250413403585