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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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DAH CARE Nitrile — 5 UDI-DI variants, MDR (MCL Group srl)

MD Atlas
MCL Group srl

Data from EUDAMED, last updated May 31, 2026

DAH CARE Nitrile

805977798DCGLOVE3201GB

5 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: MCL Group srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805977798DCGLOVE3201GB
Device name: DAH CARE Nitrile
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: MCL Group srl
SRN: IT-MF-000049484
Country: Italy
Email: info@mcl-group.it

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K5BZB11YTFD3D0DPJ6JTRSAC

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

30.3.32.01 S08059777981892
30.3.32.01 XL08059777981922
30.3.32.01 L08059777981915
30.3.32.01 M08059777981908
30.3.32.01 XS08059777983971