Taiwan FDA registration dae477e107588508836abddfd8870064
"ASKLEPION" Vaginal Discharge Self-Test (Non-Sterile)
TW: "亞斯克" 陰道分泌物PH值檢驗棒 (未滅菌)
Taiwan·Risk Class 1·MD·COMMON SENSE LTD·Registered Apr 28, 2015 – Apr 28, 2020CancelledRegistration details
- Analysis ID
- dae477e107588508836abddfd8870064
- License Form
- Ministry of Health Medical Device Import No. 015164
- Customs Code
- DHA09401516408
Company information
- Manufacturer
- COMMON SENSE LTD
- Manufacturer Country
- Israel
- Authorized Representative
- ASKLEPION BIOTECH CO., LTD.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1550 Uric pH (non-quantitative) test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 28, 2015
- Expiry Date
- Apr 28, 2020
- 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 "ASKLEPION" Vaginal Discharge Self-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 dae477e107588508836abddfd8870064 and manufactured by COMMON SENSE LTD. The authorized representative in Taiwan is ASKLEPION BIOTECH CO., LTD..
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