gudid
Primary ID: 7202
Hobbs Medical Polypectomy Snare (UDI 7202)
Manufactured by HOBBS MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hobbs Medical Polypectomy Snare - Primary ID 7202
Device Regulatory Overview
The Hobbs Medical Polypectomy Snare (Model/Catalog Number: 7202) is a medical device manufactured by HOBBS MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification OCZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7202
- Product Code / EMDN
- OCZ
- Device Name
- A flexible device intended to be inserted through an endoscope to ligate, cauterize, and cut polyps, or other mucosal lesions in the gastrointestinal (GI) tract, using high frequency current during endotherapy. It consists of a flexible insulated insertion sheath, a snare loop attached to the distal end of the sheath, and an operating wire connected to both the loop and a handle which controls the operating wire. The proximal end of the operating wire is connected to a high frequency power supply unit. 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 Medical Polypectomy Snare?
The registered manufacturer of record for Hobbs Medical Polypectomy Snare is HOBBS MEDICAL, INC..
What is the Primary UDI-DI identifier for Hobbs Medical Polypectomy Snare?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7202.
What classification code is assigned to this device?
This device is registered under product classification code OCZ.
Similar Classification Devices (OCZ)
Other Devices by HOBBS MEDICAL, INC.
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