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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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Shockwave therapy device — 3 UDI-DI variants, MDR (Likamed GmbH)

MD Atlas
Likamed GmbH

Data from EUDAMED, last updated May 23, 2026

Shockwave therapy device

42605074500000005VK

3 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: Likamed GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42605074500000005VK
Device name: Shockwave therapy device
Device model: Shockwave therapy device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 2, 2023

Manufacturer & authorised representative

Manufacturer

Name: Likamed GmbH
SRN: DE-MF-000006475
Country: Germany
Email: sebastian.lipp@likamed.de
Phone: +49 7262 91890

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GR8G08MDNGY6SA48E5Z73G8N

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

34-00-1004260507450319
30-01-2104260507450043
30-01-2204260507450050