Taiwan FDA registration 490f17e7e46aa60ddf395abe308c381e
"Seegene" Mycoplasma Pneumoniae Test (non-sterile)
TW: "視基" 肺炎黴漿菌檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·SEEGENE INC.·Registered Apr 08, 2016 – Apr 08, 2021CancelledRegistration details
- Analysis ID
- 490f17e7e46aa60ddf395abe308c381e
- License Form
- Ministry of Health Medical Device Import No. 016372
- Customs Code
- DHA09401637207
Company information
- Manufacturer
- SEEGENE INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3375 Mycoplasma serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 08, 2016
- Expiry Date
- Apr 08, 2021
- Cancellation Date
- Feb 21, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Seegene" Mycoplasma Pneumoniae 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 490f17e7e46aa60ddf395abe308c381e and manufactured by SEEGENE INC.. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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