gudid
Primary ID: 6023
Hobbs Biliary Pigtail Stent Kit (UDI 6023)
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 Pigtail Stent Kit - Primary ID 6023
Device Regulatory Overview
The Hobbs Biliary Pigtail Stent Kit (Model/Catalog Number: 6023) 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
- 6023
- Product Code / EMDN
- FGE
- Device Name
- Biliary Pigtail Stent Kit includes Stent, Guide Wire, Push Catheter and Guide Catheter.
- Database Sync Date
- 2026-08-09 09:53:53
Full Regulatory Attributes
🔒 Token Gated
{
"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 Pigtail Stent Kit?
The registered manufacturer of record for Hobbs Biliary Pigtail Stent Kit is HOBBS MEDICAL, INC..
What is the Primary UDI-DI identifier for Hobbs Biliary Pigtail Stent Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6023.
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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