Taiwan FDA registration e016c3b7c0d28fad45253eaaa83f0a22
Portable ultrasound viewer
TW: 手提超音波看診器
Registration details
- Analysis ID
- e016c3b7c0d28fad45253eaaa83f0a22
- Customs Code
- DHA00600531602
Company information
- Manufacturer
- DYMAX CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- HI-LYTE ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- 1207 ultrasonic real-time diagnostic device
- Import Information
- import
Dates and status
- Registration Date
- Aug 04, 1988
- Expiry Date
- Aug 04, 1993
- Cancellation Date
- Aug 28, 2000
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Portable ultrasound viewer in Taiwan's medical device market through Pure Global AI's free database. is registered under number e016c3b7c0d28fad45253eaaa83f0a22 and manufactured by DYMAX CORPORATION. The authorized representative in Taiwan is HI-LYTE ENTERPRISE CO., LTD..
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