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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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HNO Behandlungsstühle — 3 UDI-DI variants, MDR (Jörg & Sohn GmbH)

MD Atlas
Jörg & Sohn GmbH

Data from EUDAMED, last updated May 23, 2026

HNO Behandlungsstühle

42517328HN0SS

3 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: Jörg & Sohn GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42517328HN0SS
Device name: HNO Behandlungsstühle
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: Jörg & Sohn GmbH
SRN: DE-MF-000011346
Country: Germany
Email: info@joergundsohn.de
Phone: +499561829900

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GS5D2DC4WNVKKAZY3QY6WVKA

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

5106/104251732800048
5104/404251732800031
5101/304251732800024