Taiwan FDA registration 1c8f6fde263a8525e4374b24e05e3433
"Jester" Dental Implant Operating Equipment (Unsterilized)
TW: "傑斯特" 牙齒骨內植入物操作器材(未滅菌)
Registration details
- Analysis ID
- 1c8f6fde263a8525e4374b24e05e3433
- Customs Code
- DHA09402297803
Company information
- Manufacturer Country
- United States
- Authorized Representative
- HOWSHINE ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Dental Bone Implant Operation Equipment (F.3980)" Identification Scope of the First Level.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3980 Intradental implant manipulation equipment
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 09, 2022
- Expiry Date
- Dec 09, 2027
About this record
Access comprehensive regulatory information for "Jester" Dental Implant Operating Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1c8f6fde263a8525e4374b24e05e3433 and manufactured by ZEST ANCHORS, LLC ALSO DBA ZEST DENTAL SOLUTIONS AND DANVILLE MATERIALS. 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