Taiwan FDA registration 072298361e52cbfe8a392ac4c8fcfe7f
"HSIANG-HAO" Ovulation Test (Non-Sterile)
TW: "享豪"排卵測試筆(未滅菌)
Taiwan·Risk Class 1·MD·SPD Swiss Precision Diagnostics GmbH·Registered Dec 01, 2014 – Dec 01, 2019CancelledRegistration details
- Analysis ID
- 072298361e52cbfe8a392ac4c8fcfe7f
- License Form
- Ministry of Health Medical Device Import No. 014711
- Customs Code
- DHA09401471106
Company information
- Manufacturer
- SPD Swiss Precision Diagnostics GmbH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Xianghao Medical Equipment Co., Ltd
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1485 Luteinizing Gonadotropin Test System
Dates and status
- Registration Date
- Dec 01, 2014
- Expiry Date
- Dec 01, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "HSIANG-HAO" Ovulation Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 072298361e52cbfe8a392ac4c8fcfe7f and manufactured by SPD Swiss Precision Diagnostics GmbH. The authorized representative in Taiwan is Xianghao Medical Equipment Co., Ltd.
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