gudid
Primary ID: 102410
Injector (UDI 102410)
Manufactured by Bracco Injeneering SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Injector - Primary ID 102410
Device Regulatory Overview
The Injector (Model/Catalog Number: 102410) is a medical device manufactured by Bracco Injeneering SA. This product is indexed under FDA Product Code / Category Classification JAK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 102410
- Product Code / EMDN
- JAK
- Device Name
- Database Sync Date
- 2026-08-09 09:21:51
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 Injector?
The registered manufacturer of record for Injector is Bracco Injeneering SA.
What is the Primary UDI-DI identifier for Injector?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 102410.
What classification code is assigned to this device?
This device is registered under product classification code JAK.
Similar Classification Devices (JAK)
Other Devices by Bracco Injeneering SA
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