Taiwan FDA registration 4f9c518822f488270d1449bfb7ac216a
"Zest" Precision attachment (Non-Sterile)
TW: "傑仕德" 精密接著體 (未滅菌)
Taiwan·Risk Class 1·MD·ZEST ANCHORS, LLC·Registered Dec 28, 2015 – Dec 28, 2025ExpiredRegistration details
- Analysis ID
- 4f9c518822f488270d1449bfb7ac216a
- License Form
- Ministry of Health Medical Device Import No. 016021
- Customs Code
- DHA09401602104
Company information
- Manufacturer
- ZEST ANCHORS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Limited to the first level identification range of the "Precision Adhesive Body (F.3165)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3165 precision bond
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 28, 2015
- Expiry Date
- Dec 28, 2025
About this record
Access comprehensive regulatory information for "Zest" Precision attachment (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 4f9c518822f488270d1449bfb7ac216a and manufactured by ZEST ANCHORS, LLC. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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