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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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Mycosan Gel — 5 UDI-DI variants, MDR (Serrix B.V)

MD Atlas
Serrix B.V

Data from EUDAMED, last updated May 30, 2026

Mycosan Gel

871830970M2X0EGCW

5 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: Serrix B.V

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871830970M2X0EGCW
Device name: Mycosan Gel
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 27, 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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KJFJYDY76DJ41WBNC0WVM8SY

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

M260ES08718309703011
Mycosan Athlete's Foot - 15 mL Brushtube08718309701253
M260FI08718309703448
M260NL08718309700522
M260PT08718309703363