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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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IH 60 — 2 UDI-DI variants, MDR (Beurer GmbH)

MD Atlas
Beurer GmbH

Data from EUDAMED, last updated May 23, 2026

IH 60

4211125IH60NP

2 UDI-DI variants

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

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

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 4211125IH60NP
Device name: —
Device model: IH 60
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: Beurer GmbH
SRN: DE-MF-000005422
Country: Germany
Email: info@beurer.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JDHPYEQRKANY2HAT5W5K70CB

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

6099304211125609931
6020604211125602062