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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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Mask — 6 UDI-DI variants, MDR (medin Medical Innovations GmbH)

MD Atlas
medin Medical Innovations GmbH

Data from EUDAMED, last updated May 23, 2026

Mask

4060139000012B

6 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: medin Medical Innovations GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4060139000012B
Device name: Mask
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: medin Medical Innovations GmbH
SRN: DE-MF-000006975
Country: Germany
Email: info@medin-medical.com
Phone: +49 8142 448460

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KPN4ZP0W5JBSQ6ABJSX1M2EY

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

1200-0604060139100640
1200-0904060139101128
1200-0504060139100633
1200-0404060139100626
1200-0704060139100657
1200-0804060139100619