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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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Forceps, laryngoscopy — 2 UDI-DI variants, MDR

MD Atlas
KARL STORZ SE & Co. KG

Data from EUDAMED, last updated May 23, 2026

Forceps, laryngoscopy

4048551001478UC

2 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: 4048551001478UC
Device name: Forceps, laryngoscopy
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

2 UDI-DI variants

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Applied filters

basicUdiUlid01KS0355YHS26W4XRNB19TDEKZ

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

80912004048551312889
80912504048551010822