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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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Lang-Stereotest — 6 UDI-DI variants, MDR (Lang-Stereotest AG)

MD Atlas
Lang-Stereotest AG

Data from EUDAMED, last updated May 23, 2026

Lang-Stereotest

7649996943002KU

6 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: Lang-Stereotest AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7649996943002KU
Device name: Lang-Stereotest
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: Lang-Stereotest AG
SRN: CH-MF-000029998
Country: Switzerland
Email: info@lang-stereotest.com
Phone: +41449106139

Authorised representative

Name: Annemarie Lang-Lieder
SRN: AT-AR-000013005
Country: Austria
Phone: +4369917127590

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KP3R4JN88J4292Y2GXGVFVW1

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

REF 80207649996943088
REF 80107649996943071
REF 90107649996943095
REF 50107649996943101
REF 10307649996943057
REF 10407649996943064