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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

640076 — Class I MDR by Bracco Injeneering SA

MD Atlas
Bracco Injeneering SA

EUDAMED last updated this device on Apr 30, 2026

640076

76300393300000KF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bracco Injeneering SA
UDI-DI code: 17630039301214
Reference / catalog number: 640076

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Manufacturer information

Organization name: Bracco Injeneering SA
SRN: CH-MF-000019387
Manufacturer status: Active

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 Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	May 1, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 17630039301214
Basic UDI-DI: 76300393300000KF
Reference / catalog number: 640076
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: CT Expres Floor Stand
Additional information URL: https://eifu.braccomedtech.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11039014MULTIPLE CONTRAST AGENT INJECTORS

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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

CT Expres 4DB-47630039301932On the market CT Expres EvoB-47630039302106On the market 650600B-CH-MF-000019387KEOn the market 64065076300393300000KFOn the market CT Expres Multi Patient SetB-37630039301522On 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.