eudamed_udi
Primary ID: 37630039301539
CT Expres Patient Line (UDI 37630039301539)
Manufactured by Bracco Injeneering SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CT Expres Patient Line - Primary ID 37630039301539
Device Regulatory Overview
The CT Expres Patient Line (Model/Catalog Number: 640063) is a medical device manufactured by Bracco Injeneering SA. This product is indexed under FDA Product Code / Category Classification Z11039014 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 640063
- Product Code / EMDN
- Z11039014
- Device Name
- CT Expres Patient Line
- Database Sync Date
- 2026-08-09 18:27:09
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of CT Expres Patient Line?
The registered manufacturer of record for CT Expres Patient Line is Bracco Injeneering SA.
What is the Primary UDI-DI identifier for CT Expres Patient Line?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 37630039301539.
What classification code is assigned to this device?
This device is registered under product classification code Z11039014.
Similar Classification Devices (Z11039014)
Other Devices by Bracco Injeneering SA
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