gudid
Primary ID: 6552
Freeman Pancreatic Flexi-Stent (UDI 6552)
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 - Primary ID 6552
Device Regulatory Overview
The Freeman Pancreatic Flexi-Stent (Model/Catalog Number: 6552) 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
- 6552
- Product Code / EMDN
- FGE
- Device Name
- A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed pancreatic duct (e.g., due to stricture or malignancy) to maintain luminal patency; it may also be intended to treat a wide variety of conditions in pancreatic endoscopy (e.g., drain pseudocyst, treat fistula or duct disruption). It is made entirely of a synthetic polymer and has a continuous tube design with or without retention flanges. 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?
The registered manufacturer of record for Freeman Pancreatic Flexi-Stent is HOBBS MEDICAL, INC..
What is the Primary UDI-DI identifier for Freeman Pancreatic Flexi-Stent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6552.
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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