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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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Detalo Clinical — 2 UDI-DI variants, MDR (Detalo Health ApS)

MD Atlas
Detalo Health ApS

Data from EUDAMED, last updated May 31, 2026

Detalo Clinical

57000022676DC-CSERIES01ML

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: Detalo Health ApS

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Device characteristics

Active deviceMeasuring function

Clinical investigations

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 57000022676DC-CSERIES01ML
Device name: Detalo Clinical
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 31, 2023

Manufacturer & authorised representative

Manufacturer

Name: Detalo Health ApS
SRN: DK-MF-000035616
Country: Denmark
Email: contact@detalo-health.com
Phone: +4540105169

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HDPJW5ADM2D1SZ8G5BHRXM1Z

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

S2481705700002267610
S2437105700002267603