Taiwan FDA registration 0cf456b3b03ff750d95d2749e13fef83
“Huntleigh” Doppler Fetal Detector
TW: “杭特萊”都卜勒胎兒心音偵測器
Taiwan·Risk Class 2·MD·HUNTLEIGH HEALTHCARE LTD., DIAGNOSTIC PRODUCTS DIVISION·Registered Sep 21, 2018 – Sep 21, 2023ExpiredRegistration details
- Analysis ID
- 0cf456b3b03ff750d95d2749e13fef83
- License Form
- Ministry of Health Medical Device Import No. 031529
- Customs Code
- DHA05603152907
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 Devices for obstetrics and gynecology
- Product Type (Level 2)
- L2660 Fetal ultrasound monitor and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 21, 2018
- Expiry Date
- Sep 21, 2023
About this record
Access comprehensive regulatory information for “Huntleigh” Doppler Fetal Detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0cf456b3b03ff750d95d2749e13fef83 and manufactured by HUNTLEIGH HEALTHCARE LTD., DIAGNOSTIC PRODUCTS DIVISION. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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