gudid
Primary ID: 6521
Freeman Pancreatic Flexi-Stent Kit (UDI 6521)
Manufactured by HOBBS MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Freeman Pancreatic Flexi-Stent Kit - Primary ID 6521
Device Regulatory Overview
The Freeman Pancreatic Flexi-Stent Kit (Model/Catalog Number: 6521) 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
- 6521
- Product Code / EMDN
- FGE
- Device Name
- Pancreatic Flexi-Stent Kit includes Stent and Pusher Catheter. This is a single-use device.
- 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 Freeman Pancreatic Flexi-Stent Kit?
The registered manufacturer of record for Freeman Pancreatic Flexi-Stent Kit is HOBBS MEDICAL, INC..
What is the Primary UDI-DI identifier for Freeman Pancreatic Flexi-Stent Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6521.
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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