K Files (UDI 06942200940059)
Manufactured by Shanwei Perfect Medical Instruments Co.,Ltd.
Device Regulatory Overview
The K Files (Model/Catalog Number: A330 650 926 2802 006) is a medical device manufactured by Shanwei Perfect Medical Instruments 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
- A330 650 926 2802 006
- Product Code / EMDN
- Q010507
- Device Name
- Dental Root-Canal Instruments
- Database Sync Date
- 2026-08-09 16:28:44
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 K Files?
The registered manufacturer of record for K Files is Shanwei Perfect Medical Instruments Co.,Ltd..
What is the Primary UDI-DI identifier for K Files?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942200940059.
What classification code is assigned to this device?
This device is registered under product classification code Q010507.
Similar Classification Devices (Q010507)
Other Devices by Shanwei Perfect Medical Instruments Co.,Ltd.
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