gudid
Primary ID: 6113
Hobbs Biliary Amsterdam Stent (UDI 6113)
Manufactured by HOBBS MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hobbs Biliary Amsterdam Stent - Primary ID 6113
Device Regulatory Overview
The Hobbs Biliary Amsterdam Stent (Model/Catalog Number: 6113) is a medical device manufactured by HOBBS MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification FGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6113
- Product Code / EMDN
- FGE
- Device Name
- A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed biliary duct (e.g., common bile duct) to maintain luminal patency. It is made entirely of a synthetic polymer designed as a continuous tube with retention flanges. Single use device.
- Database Sync Date
- 2026-08-09 09:53:53
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 Hobbs Biliary Amsterdam Stent?
The registered manufacturer of record for Hobbs Biliary Amsterdam Stent is HOBBS MEDICAL, INC..
What is the Primary UDI-DI identifier for Hobbs Biliary Amsterdam Stent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6113.
What classification code is assigned to this device?
This device is registered under product classification code FGE.
Similar Classification Devices (FGE)
Other Devices by HOBBS MEDICAL, INC.
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