Taiwan FDA registration 1701f747589ef11ff9fdcbf701eeffa0
"Kentley" Herojan periodontal probe
TW: 〝肯特利〞摩洛珍牙周探針
Taiwan·Risk Class 1·KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP·Registered Oct 31, 2005 – Oct 31, 2010CancelledRegistration details
- Analysis ID
- 1701f747589ef11ff9fdcbf701eeffa0
- Customs Code
- DHA04400163502
Company information
- Manufacturer
- KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Tyco Pharmaceutical Co., Ltd
Product details
- Intended Use
- Hand dental instruments are hand-held instruments used to perform various procedures in general dentistry and oral surgery.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- import
Dates and status
- Registration Date
- Oct 31, 2005
- Expiry Date
- Oct 31, 2010
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kentley" Herojan periodontal probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1701f747589ef11ff9fdcbf701eeffa0 and manufactured by KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP. The authorized representative in Taiwan is Taiwan Tyco Pharmaceutical 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