Taiwan FDA registration 423acdf42b218fa1b91f02c2a3a568bc
"Zest" Dental operative unit and accessories (Non-Sterile)
TW: "傑斯特" 牙科手術裝置及其附件 (未滅菌)
Registration details
- Analysis ID
- 423acdf42b218fa1b91f02c2a3a568bc
- License Form
- Ministry of Health Medical Device Import No. 017663
- Customs Code
- DHA09401766300
Company information
- Manufacturer
- ZEST ANCHORS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- HOWSHINE ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6640 Dental Surgical Devices and Their Accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 30, 2017
- Expiry Date
- Mar 30, 2022
About this record
Access comprehensive regulatory information for "Zest" Dental operative unit and accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 423acdf42b218fa1b91f02c2a3a568bc and manufactured by ZEST ANCHORS, LLC. The authorized representative in Taiwan is HOWSHINE ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices