Taiwan FDA registration 7ff01a0fab6fd82215ba17f4c8baeaea
Defibrillation shock machine
TW: 去顫電擊機
Taiwan·LAERDAL MANUFACTURING CORPORATION·Registered Jan 20, 1992 – Jan 20, 1997CancelledRegistration details
- Analysis ID
- 7ff01a0fab6fd82215ba17f4c8baeaea
- Customs Code
- DHA00600655700
Company information
- Manufacturer
- LAERDAL MANUFACTURING CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Tomoh Limited
Product details
- Product Type (Level 1)
- 0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Jan 20, 1992
- Expiry Date
- Jan 20, 1997
- Cancellation Date
- Oct 07, 1999
Cancellation information
- Status
- Logged out
- Reason
- 改列無須辦理查驗之醫療器材;;未展延而逾期者
About this record
Access comprehensive regulatory information for Defibrillation shock machine in Taiwan's medical device market through Pure Global AI's free database. is registered under number 7ff01a0fab6fd82215ba17f4c8baeaea and manufactured by LAERDAL MANUFACTURING CORPORATION. The authorized representative in Taiwan is Tomoh Limited.
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