Taiwan FDA registration 2561c4af3a7cdcc256795cf8dec71f51
“ Zest” Locator Implant Abutment
TW: “傑思特”牙科用植體基柱
Taiwan·Risk Class 2·MD·ZEST ANCHORS LLC·Registered Oct 06, 2016 – Oct 06, 2021ExpiredRegistration details
- Analysis ID
- 2561c4af3a7cdcc256795cf8dec71f51
- License Form
- Ministry of Health Medical Device Import No. 028853
- Customs Code
- DHA05602885306
Company information
- Manufacturer
- ZEST ANCHORS LLC
- Manufacturer Country
- United States
- Authorized Representative
- PMCJ TECH COMPANY, LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3630 Dental bridges for bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 06, 2016
- Expiry Date
- Oct 06, 2021
About this record
Access comprehensive regulatory information for “ Zest” Locator Implant Abutment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2561c4af3a7cdcc256795cf8dec71f51 and manufactured by ZEST ANCHORS LLC. The authorized representative in Taiwan is PMCJ TECH COMPANY, 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