Taiwan FDA registration f43d162f0c23b13363091ea38a752025
Cardiac flow Semi-automatic extracorporeal cardiac defibrous fibrillators
TW: 心流 半自動體外心臟去纖維顫動器
Taiwan·HEARTSTREAM INC.·Registered Oct 17, 1997 – Oct 17, 2002CancelledRegistration details
- Analysis ID
- f43d162f0c23b13363091ea38a752025
- Customs Code
- DHA00600843002
Company information
- Manufacturer
- HEARTSTREAM INC.
- Manufacturer Country
- United States
- Authorized Representative
- TAIWAN HOSPITAL SUPPLY CORPORATION
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- 0619 Intensive Care Unit & Cardiac Intensive Care Unit Leadwires & Electrodes
- Import Information
- import
Dates and status
- Registration Date
- Oct 17, 1997
- Expiry Date
- Oct 17, 2002
- Cancellation Date
- Dec 13, 2004
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Cardiac flow Semi-automatic extracorporeal cardiac defibrous fibrillators in Taiwan's medical device market through Pure Global AI's free database. is registered under number f43d162f0c23b13363091ea38a752025 and manufactured by HEARTSTREAM INC.. The authorized representative in Taiwan is TAIWAN HOSPITAL SUPPLY CORPORATION.
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