Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

017416 — Class I MDR by Bracco Injeneering SA

MD Atlas
Bracco Injeneering SA

EUDAMED last updated this device on May 1, 2026

017416

76300393100000JM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bracco Injeneering SA
UDI-DI code: 37630039300617
Reference / catalog number: 017416

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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 2 countries total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market
Austria		Still on market

Device identification

Trade name: not provided
UDI-DI code: 37630039300617
Basic UDI-DI: 76300393100000JM
Reference / catalog number: 017416
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: EmpowerCTA+ Articulating Arm
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 64007676300393300000KFOn the market 64065076300393300000KFOn 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.