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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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Detall — 1 UDI-DI variant, MDR (HÄLSA Pharma GmbH)

MD Atlas
HÄLSA Pharma GmbH

Data from EUDAMED, last updated May 31, 2026

Detall

42517781MD229CY

1 UDI-DI variant

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42517781MD229CY
Device name: —
Device model: Detall
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: HÄLSA Pharma GmbH
SRN: DE-MF-000007407
Country: Germany
Email: info@haelsa.de

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KS82B1BXX7NH175VWS157B9X

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

Detall04251778101710