Disposable Non-electric Biopsy Forceps (UDI VDK-FB-23-230-O-P1-A2)
Manufactured by Jiangsu Vedkang Medical Science and Technology Co.,Ltd.
Device Regulatory Overview
The Disposable Non-electric Biopsy Forceps (Model/Catalog Number: VDK-FB-23-230-O-P1-A2) is a medical device manufactured by Jiangsu Vedkang Medical Science and Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification FCL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VDK-FB-23-230-O-P1-A2
- Product Code / EMDN
- FCL
- Device Name
- Database Sync Date
- 2026-08-09 09:04:50
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 Disposable Non-electric Biopsy Forceps?
The registered manufacturer of record for Disposable Non-electric Biopsy Forceps is Jiangsu Vedkang Medical Science and Technology Co.,Ltd..
What is the Primary UDI-DI identifier for Disposable Non-electric Biopsy Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VDK-FB-23-230-O-P1-A2.
What classification code is assigned to this device?
This device is registered under product classification code FCL.
Similar Classification Devices (FCL)
Other Devices by Jiangsu Vedkang Medical Science and Technology Co.,Ltd.
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