Taiwan FDA registration 62d3b8751fe8b22f1a84885f5fd5a1aa
"UNIPATH" Ovulation Test (Non-Sterile)
TW: "優妳佩" 排卵測試筆(未滅菌)
Taiwan·Risk Class 1·MD·UNIPATH LIMITED·Registered Oct 15, 2014 – Oct 15, 2019CancelledRegistration details
- Analysis ID
- 62d3b8751fe8b22f1a84885f5fd5a1aa
- License Form
- Ministry of Health Medical Device Import No. 014574
- Customs Code
- DHA09401457409
Company information
- Manufacturer
- UNIPATH LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- WEIYOU TECH INC.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1485 Luteinizing Gonadotropin Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 15, 2014
- Expiry Date
- Oct 15, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "UNIPATH" 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 62d3b8751fe8b22f1a84885f5fd5a1aa and manufactured by UNIPATH LIMITED. The authorized representative in Taiwan is WEIYOU TECH INC..
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