Taiwan FDA registration 0fab7d7662935d824a62436577b79ca9
Single, bi- and triple-circuit right arterial ductus
TW: 單、雙、三迴路右動脈導管
Taiwan·QUINTON INSTRUMENT CO.·Registered Aug 04, 1995 – Aug 04, 2000CancelledRegistration details
- Analysis ID
- 0fab7d7662935d824a62436577b79ca9
- Customs Code
- DHA00600757800
Company information
- Manufacturer
- QUINTON INSTRUMENT CO.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Tyco Pharmaceutical Co., Ltd
Product details
- Product Type (Level 1)
- 0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Aug 04, 1995
- Expiry Date
- Aug 04, 2000
- Cancellation Date
- Dec 14, 2004
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Single, bi- and triple-circuit right arterial ductus in Taiwan's medical device market through Pure Global AI's free database. is registered under number 0fab7d7662935d824a62436577b79ca9 and manufactured by QUINTON INSTRUMENT CO.. The authorized representative in Taiwan is Taiwan Tyco Pharmaceutical Co., Ltd.
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