Taiwan FDA registration 80874a237e1abea5ddecd45b946ba7e4
"Sonygot" fetal monitoring instrument
TW: "索尼格特" 胎兒監視儀器
Taiwan·Risk Class 2·HUNTLEIGH HEALTHCARE LTD., DIAGNOSTIC PRODUCTS DIVISION·Registered Nov 02, 2005 – Nov 02, 2015CancelledRegistration details
- Analysis ID
- 80874a237e1abea5ddecd45b946ba7e4
- Customs Code
- DHA00601288200
Company information
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TRUSHINE MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Import Information
- import
Dates and status
- Registration Date
- Nov 02, 2005
- Expiry Date
- Nov 02, 2015
- Cancellation Date
- May 10, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Sonygot" fetal monitoring instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 80874a237e1abea5ddecd45b946ba7e4 and manufactured by HUNTLEIGH HEALTHCARE LTD., DIAGNOSTIC PRODUCTS DIVISION. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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