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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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Pregnolia Control Unit — 4 UDI-DI variants, MDR (Pregnolia AG)

MD Atlas
Pregnolia AG

Data from EUDAMED, last updated May 23, 2026

Pregnolia Control Unit

7649998703PregCUSY

4 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: Pregnolia AG

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 7649998703PregCUSY
Device name: Pregnolia Control Unit
Device model: 100058
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Pregnolia AG
SRN: CH-MF-000033377
Country: Switzerland
Email: info@pregnolia.com

Authorised representative

Name: Medical Technology Promedt Consulting GmbH
SRN: DE-AR-000000085
Country: Germany
Phone: +49 6894 581020

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KGSQKFAW5Y7FM6CXS9M99T97

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

10005807649998703116
10005807649998703086
10004407649998703079
10004407649998703123