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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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Eczema Repair — 1 UDI-DI variant, MDR (Serrix B.V)

MD Atlas
Serrix B.V

Data from EUDAMED, last updated May 31, 2026

Eczema Repair

871830970D0X0EG8K

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: Serrix B.V

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871830970D0X0EG8K
Device name: Eczema Repair
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Serrix B.V
SRN: NL-MF-000005882
Country: Netherlands
Email: quality@serrix.com
Phone: +31203378703

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KHX35224P7CAN8P32WBJFF7G

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

D060NL08718309701079