Taiwan FDA registration 78f08e1b848e864c8002789ae7b8d93e
"Meridian" sleep physiology detector
TW: “經絡”睡眠生理檢測器
Taiwan·Risk Class 2·Meridian Power Medical Co., Ltd. Xizhi Factory·Registered Jun 20, 2007 – Jun 20, 2012CancelledRegistration details
- Analysis ID
- 78f08e1b848e864c8002789ae7b8d93e
- Customs Code
- DHY00500222503
Company information
- Manufacturer
- Meridian Power Medical Co., Ltd. Xizhi Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Meridian Power Medical Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.2375 Respiratory frequency monitor
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 20, 2007
- Expiry Date
- Jun 20, 2012
- Cancellation Date
- Apr 14, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Meridian" sleep physiology detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78f08e1b848e864c8002789ae7b8d93e and manufactured by Meridian Power Medical Co., Ltd. Xizhi Factory. The authorized representative in Taiwan is Meridian Power Medical Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices