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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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Footswitches — 3 UDI-DI variants, MDR (KARL STORZ SE & Co. KG)

MD Atlas
KARL STORZ SE & Co. KG

Data from EUDAMED, last updated May 23, 2026

Footswitches

4048551001855UL

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: KARL STORZ SE & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 4048551001855UL
Device name: Footswitches
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: KARL STORZ SE & Co. KG
SRN: DE-MF-000005723
Country: Germany
Email: regulatory@karlstorz.com
Phone: +49 (0)7461 708-0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2KT45DB1CPQP54T3T53X01

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

UF201W04048551435410
UF102W04048551435434
UF101W04048551435380