gudid
Primary ID: ZBM12060
ELuminexx Biliary Stent (UDI ZBM12060)
Manufactured by Bard Peripheral Vascular, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELuminexx Biliary Stent - Primary ID ZBM12060
Device Regulatory Overview
The ELuminexx Biliary Stent (Model/Catalog Number: ZBM12060) is a medical device manufactured by Bard Peripheral Vascular, Inc.. This product is indexed under FDA Product Code / Category Classification FGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZBM12060
- Product Code / EMDN
- FGE
- Device Name
- ELuminexx Biliary Stent 12 mm x 60 mm (80 cm delivery catheter)
- Database Sync Date
- 2026-08-09 09:11:22
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ELuminexx Biliary Stent?
The registered manufacturer of record for ELuminexx Biliary Stent is Bard Peripheral Vascular, Inc..
What is the Primary UDI-DI identifier for ELuminexx Biliary Stent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZBM12060.
What classification code is assigned to this device?
This device is registered under product classification code FGE.
Similar Classification Devices (FGE)
Other Devices by Bard Peripheral Vascular, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint