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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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Organization name
UDI-DI code
Reference / catalog number

100044 — Class I MDR by Pregnolia AG

MD Atlas
Pregnolia AG

EUDAMED last updated this device on Feb 9, 2026

100044

7649998703PregCUSY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Pregnolia AG
UDI-DI code: 07649998703079
Reference / catalog number: 100044

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Manufacturer information

Organization name: Pregnolia AG
SRN: CH-MF-000033377
Manufacturer status: Active

Related devices

100058B-CHMF000033377PregCUQSOn the market 1000587649998703PregCUSYOn the market 1000587649998703PregCUSYOn the market 1000447649998703PregCUSYOn the market 2000147649998703PregPROHVOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 07649998703079
Basic UDI-DI: 7649998703PregCUSY
Reference / catalog number: 100044
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Firmware FW 2.01
Additional information URL: https://en.pregnolia.com/instructions
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V030205OBSTETRICS AND GYNECOLOGY MEASUREMENT DEVICES NOT INCLUDED IN OTHER CLASSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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Software identification