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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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Ingrown nails serum — 2 UDI-DI variants, MDR

MD Atlas
Swiss Footcare Laboratories sarl

Data from EUDAMED, last updated May 23, 2026

Ingrown nails serum

764017821APAISANTPO2Q

2 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: Swiss Footcare Laboratories sarl

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Device characteristics

No device characteristics flagged

Clinical investigations

Investigation number: 23E2009
Registered: No

Identity & classification

Basic UDI-DI: 764017821APAISANTPO2Q
Device name: Ingrown nails serum
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Swiss Footcare Laboratories sarl
SRN: CH-MF-000045926
Country: Switzerland
Email: contact@poderm.com

Authorised representative

Name: AF Pharma Service Europe SL
SRN: ES-AR-000018076
Country: Spain

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JPMZS2GN7VQGKP90HS09RQNX

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

PODERM Ingrown toe Nail serum07640178212190
PODERM Soothing serum Ingrown toeNails07640178210028