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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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Pregnenolone sulfate LC-MS/MS — 3 UDI-DI variants, IVDR

MD Atlas
Immundiagnostik AG

Data from EUDAMED, last updated May 23, 2026

Pregnenolone sulfate LC-MS/MS

4050598DVPhysiolW8

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class B

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: Immundiagnostik AG

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Device characteristics

Professional testingHuman tissues / cells

Identity & classification

Basic UDI-DI: 4050598DVPhysiolW8
Device name: Pregnenolone sulfate LC-MS/MS
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Jun 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: Immundiagnostik AG
SRN: DE-MF-000020905
Country: Germany
Email: info@immundiagnostik.com
Phone: +496251701900

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JYE2YRYWTNGAEJAD8TZ56K00

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

YM2000CAL1-604050598014145
YM2000CTRL1-304050598014152
YM200004050598012707