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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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Forwarts Wart Remover — 8 UDI-DI variants, MDR

MD Atlas
Pronova Laboratories BV

Data from EUDAMED, last updated May 31, 2026

Forwarts Wart Remover

871734439FW10XXJ9

8 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: Pronova Laboratories BV

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 871734439FW10XXJ9
Device name: Forwarts Wart Remover
Device model: FW10XX100
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: Pronova Laboratories BV
SRN: NL-MF-000001486
Country: Netherlands
Email: info@pronovalab.com
Phone: +31 294 466611

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K1TTYBTW6PCHX0P7PZST4V1E

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

Dr. Scholl's Freeze Away MAX EXPERTTREATMENT Traitement Verrues Cryothérapie08717344390620
FW10NORD10008717344390590
Dr. Scholl's Freeze Away MAX Traitement Verrues Cryothérapie08717344390613
FW10ITGR10008717344390583
FW10PLHU10008717344390637
FW10NL10008717344390170
FW10BE10008717344390286
FW10DE10008717344390019