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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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WAW Duo FUE Product line — 10 UDI-DI variants, MDR

MD Atlas
Devroye Instruments SRL

Data from EUDAMED, last updated May 23, 2026

WAW Duo FUE Product line

54300033620WDFSystem69

10 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: Devroye Instruments SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 54300033620WDFSystem69
Device name: WAW Duo FUE Product line
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Devroye Instruments SRL
SRN: BE-MF-000034423
Country: Belgium
Email: info@devroyeinstruments.com

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01HCMNJKJR7MYXWQ2Q57BZXCJ6

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

WAW Charging Station v305430003362242
WAW Duo FUE System v205430003362259
WAW Slim Handpiece V105430003362112
WAW Software V105430003362280
WAW Wireless Handpiece05430003362006
WAW Duo FUE System05430003362044
External Sleeve Support Box05430003362051
WAW Pedal05430003362020
Wired Handpiece05430003362013
WAW Charging Station05430003362037