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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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MODULITH SLX-F2 — 3 UDI-DI variants, MDR (STORZ MEDICAL AG)

MD Atlas
STORZ MEDICAL AG

Data from EUDAMED, last updated May 23, 2026

MODULITH SLX-F2

76300391ESWL002-QC

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: STORZ MEDICAL AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 76300391ESWL002-QC
Device name: MODULITH SLX-F2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: STORZ MEDICAL AG
SRN: CH-MF-000014374
Country: Switzerland
Email: info@storzmedical.com
Phone: +41 71 677 45 45

Authorised representative

Name: STORZ MEDICAL Deutschland GmbH
SRN: DE-AR-000009017
Country: Germany

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FS201ZBEK3CPSM01ZY467GZ9

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

39000.000307630039101466
39000.000207630039101459
39000.000107630039101442