Dental Diamond Burs (UDI 06978049075089)
Manufactured by Anson Investment Development Co.,Ltd.
Device Regulatory Overview
The Dental Diamond Burs (Model/Catalog Number: TF-23) is a medical device manufactured by Anson Investment Development Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification Q0199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TF-23
- Product Code / EMDN
- Q0199
- Device Name
- Dental Burs
- Database Sync Date
- 2026-08-09 16:47:15
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 Dental Diamond Burs?
The registered manufacturer of record for Dental Diamond Burs is Anson Investment Development Co.,Ltd..
What is the Primary UDI-DI identifier for Dental Diamond Burs?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978049075089.
What classification code is assigned to this device?
This device is registered under product classification code Q0199.
Similar Classification Devices (Q0199)
Other Devices by Anson Investment Development Co.,Ltd.
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