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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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GU/arm strap, single use — 4 UDI-DI variants, MDR

MD Atlas
DANISH HEALTHCARE ApS

Data from EUDAMED, last updated May 23, 2026

GU/arm strap, single use

5715005000025K

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: DANISH HEALTHCARE ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5715005000025K
Device name: GU/arm strap, single use
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: DANISH HEALTHCARE ApS
SRN: DK-MF-000001741
Country: Denmark
Email: info@danishhealthcare.com
Phone: +4521737878

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KJ7WGV6H5WN45BHCCYW9B716

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

GU/arm strap, single use05715005010101
GU/arm strap, single use05715005010088
GU/arm strap, single use05715005010095
GU/arm strap, single use05715005010118