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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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ISDIN SI-NAILS MICOXPERT MD — 5 UDI-DI variants, MDR (ISDIN, S.A)

MD Atlas
ISDIN, S.A

Data from EUDAMED, last updated May 23, 2026

ISDIN SI-NAILS MICOXPERT MD

8429420MDRTF0124P

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: ISDIN, S.A

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 8429420MDRTF0124P
Device name: ISDIN SI-NAILS MICOXPERT MD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: ISDIN, S.A
SRN: ES-MF-000003221
Country: Spain
Email: patricia.baulenas@isdin.com
Phone: +34 932402020

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HMRMVQASF7VZQM2G95F7RD81

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

69002978708429420263673
69002272308429420227231
69002636608429420263666
69002978808429420264595
69002636508429420263659