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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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SPRYSTEP MAX — 10 UDI-DI variants, MDR (Thuasne Deutschland GmbH)

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

SPRYSTEP MAX

4035459DE0904D4N

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: Thuasne Deutschland GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4035459DE0904D4N
Device name: SPRYSTEP MAX
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

10 UDI-DI variants

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Applied filters

basicUdiUlid01KBZ1N9HMMQFHKKJNCZDJVR8V

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

U017346000500104035459401289
U017346040500104035459401364
U017346030500104035459401340
U017346020500104035459401326
U017346040500204035459401371
U017346020500204035459401333
U017346030500204035459401357
U017346000500204035459401296
U017346010500104035459401302
U017346010500204035459401319