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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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Probes/Bougies/Dilators — 13 UDI-DI variants, MDR

MD Atlas
KARL STORZ SE & Co. KG

Data from EUDAMED, last updated May 23, 2026

Probes/Bougies/Dilators

4048551001441TM

13 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4048551001441TM
Device name: Probes/Bougies/Dilators
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

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS035440SM4WFXS25KFZY7XF

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

74571204048551196380
74592204048551252369
74591004048551196632
74571104048551196373
74592104048551252376
74592304048551252352
74590504048551274644
74571004048551196366
74592004048551252383
74592404048551266632
74570804048551196342
74571304048551196397
74570904048551196359