Kite Gold (UDI 06942512515419)
Manufactured by Shenzhen Denco Medical Co., Ltd.
Device Regulatory Overview
The Kite Gold (Model/Catalog Number: D-P.01.02-025-04-040-GD-000-00-00) is a medical device manufactured by Shenzhen Denco Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Q010507 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D-P.01.02-025-04-040-GD-000-00-00
- Product Code / EMDN
- Q010507
- Device Name
- 25mm 40/04 6pcs/blister
- Database Sync Date
- 2026-08-09 16:28:50
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 Kite Gold?
The registered manufacturer of record for Kite Gold is Shenzhen Denco Medical Co., Ltd..
What is the Primary UDI-DI identifier for Kite Gold?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942512515419.
What classification code is assigned to this device?
This device is registered under product classification code Q010507.
Similar Classification Devices (Q010507)
Other Devices by Shenzhen Denco Medical Co., Ltd.
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