Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Handles, dismountable instruments — 29 UDI-DI variants, MDR

MD Atlas
KARL STORZ SE & Co. KG

Data from EUDAMED, last updated May 23, 2026

Handles, dismountable instruments

4048551000787UM

29 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: KARL STORZ SE & Co. KG

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4048551000787UM
Device name: Handles, dismountable instruments
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 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

29 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KS0354QCV83DYZ9NEG1SSB0M

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

3313104048551125144
26296HM04048551067086
3315304048551009383
3316204048551328279
33151P04048551391716
3013104048551120231
33149P04048551325223
38151P04048551328866
3314704048551265123
26184HM04048551102886
3313304048551125298
3314104048551125441
3316604048551328293
26296HR04048551067109
33121W04048551125038
3314604048551265130
26167FGR04048551095324
3313204048551125281
3313904048551125397
3316104048551009406
26196HM04048551104040
30623UH04048551123683
26184HR04048551102947
33131P04048551125243
26196HR04048551104064

1 2