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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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MANU PROMASTER — 12 UDI-DI variants, MDR (Thuasne Deutschland GmbH)

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

MANU PROMASTER

4035459DE0401B36

12 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: Thuasne Deutschland GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4035459DE0401B36
Device name: MANU PROMASTER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: Thuasne Deutschland GmbH
SRN: DE-MF-000006210
Country: Germany
Email: ra@thuasne.de

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01KBZ1NA85Y313SDCFJB91X69F

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

T3507022050110204035459320504
T3507022010110204035459320429
T3507022040110104035459320474
T3507022030110204035459320467
T3507022020110104035459320436
T3507022060110204035459320528
T3507022040110204035459320481
T3507022010110104035459320412
T3507022050110104035459320498
T3507022020110204035459320443
T3507022030110104035459320450
T3507022060110104035459320511