gudid
Primary ID: G31905
Fusion (UDI G31905)
Manufactured by COOK INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fusion - Primary ID G31905
Device Regulatory Overview
The Fusion (Model/Catalog Number: G31905) is a medical device manufactured by COOK INCORPORATED. This product is indexed under FDA Product Code / Category Classification LQR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G31905
- Product Code / EMDN
- LQR
- Device Name
- Fusion Wire Guided Extraction Basket
- Database Sync Date
- 2026-08-09 09:33:19
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 Fusion?
The registered manufacturer of record for Fusion is COOK INCORPORATED.
What is the Primary UDI-DI identifier for Fusion?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G31905.
What classification code is assigned to this device?
This device is registered under product classification code LQR.
Similar Classification Devices (LQR)
Other Devices by COOK INCORPORATED
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