gudid
Primary ID: 6138
Hobbs Pusher Catheter (UDI 6138)
Manufactured by HOBBS MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hobbs Pusher Catheter - Primary ID 6138
Device Regulatory Overview
The Hobbs Pusher Catheter (Model/Catalog Number: 6138) 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
- 6138
- Product Code / EMDN
- FGE
- Device Name
- A sterile device inserted through a compatible flexible endoscope to aid in implanting a stent, typically into a pancreatic or biliary duct in order to maintain patency. It is commonly made of polytetrafluoroethylene (PTFE). This is a 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 Pusher Catheter?
The registered manufacturer of record for Hobbs Pusher Catheter is HOBBS MEDICAL, INC..
What is the Primary UDI-DI identifier for Hobbs Pusher Catheter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6138.
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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