Taiwan FDA registration c81b402e89efeb5672e9111a2d72d817
"Thermo Fisher Scientific" Legionella Test (Non-Sterile)
TW: "賽默飛世爾科技" 退伍軍人肺炎尿液抗原檢測試劑(未滅菌)
Taiwan·Risk Class 1·MD·REMEL INC.·Registered Nov 16, 2016 – Nov 16, 2021ExpiredRegistration details
- Analysis ID
- c81b402e89efeb5672e9111a2d72d817
- License Form
- Ministry of Health Medical Device Import No. 017178
- Customs Code
- DHA09401717803
Company information
- Manufacturer
- REMEL INC.
- Manufacturer Country
- United States
- Authorized Representative
- THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.
Product details
- Intended Use
- Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3300 Haemophilus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 16, 2016
- Expiry Date
- Nov 16, 2021
About this record
Access comprehensive regulatory information for "Thermo Fisher Scientific" Legionella 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 c81b402e89efeb5672e9111a2d72d817 and manufactured by REMEL INC.. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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