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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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Rigid/optical grasping forceps,… — 38 UDI-DI variants, MDR

MD Atlas
KARL STORZ SE & Co. KG

Data from EUDAMED, last updated May 23, 2026

Rigid/optical grasping forceps, bronchoscopy

4048551000105ST

38 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: 4048551000105ST
Device name: Rigid/optical grasping forceps, bronchoscopy
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

38 UDI-DI variants

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Applied filters

basicUdiUlid01KRZRR5XYDSAYHYG7VJTSWXAC

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

10372HL04048551047439
10370JL04048551047101
10371H04048551047286
10350KF04048551046715
10372K04048551047460
10378KF04048551047620
10379CF04048551047682
10350ST04048551260302
10377KF04048551047576
10374HF04048551260289
10367K04048551047019
10352H04048551046791
10371J04048551047309

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