Taiwan FDA registration bb9cc4db9617663ee9e49e2edbdf955e
"Kentley" pulp rinse syringe
TW: "肯特利"牙髓沖洗注射器
Taiwan·Risk Class 1·KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP·Registered Mar 15, 2006 – Mar 15, 2011CancelledRegistration details
- Analysis ID
- bb9cc4db9617663ee9e49e2edbdf955e
- Customs Code
- DHA04400296502
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
- Mar 15, 2006
- Expiry Date
- Mar 15, 2011
- 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" pulp rinse syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bb9cc4db9617663ee9e49e2edbdf955e and manufactured by KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP. The authorized representative in Taiwan is Taiwan Tyco Pharmaceutical Co., Ltd.
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