Taiwan FDA registration 7bb433b26f1d9361424830b14b5b5d65
"Dai Max" Seri Ultrasound Imaging System
TW: "戴麥克思" 瑟瑞超音波影像系統
Taiwan·Risk Class 2·DYMAX CORPORATION·Registered Nov 24, 2005 – Nov 24, 2015CancelledRegistration details
- Analysis ID
- 7bb433b26f1d9361424830b14b5b5d65
- Customs Code
- DHA00601367204
Company information
- Manufacturer
- DYMAX CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Import Information
- import
Dates and status
- Registration Date
- Nov 24, 2005
- Expiry Date
- Nov 24, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Dai Max" Seri Ultrasound Imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7bb433b26f1d9361424830b14b5b5d65 and manufactured by DYMAX CORPORATION. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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