Taiwan FDA registration 9a99806bd1179b88d81024de74cd632e
“Helena” Urine Protein Kit (Non-sterile)
TW: “賀蓮那”尿蛋白電泳試劑 (未滅菌)
Taiwan·Risk Class 1·MD·HELENA LABORATORIES INC.·Registered Apr 11, 2014 – Apr 11, 2019CancelledRegistration details
- Analysis ID
- 9a99806bd1179b88d81024de74cd632e
- License Form
- Ministry of Health Medical Device Import No. 014044
- Customs Code
- DHA09401404406
Company information
- Manufacturer
- HELENA LABORATORIES INC.
- Manufacturer Country
- United States
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1630 Protein (Chemical Separation) Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 11, 2014
- Expiry Date
- Apr 11, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for “Helena” Urine Protein Kit (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 9a99806bd1179b88d81024de74cd632e and manufactured by HELENA LABORATORIES INC.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..
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