Taiwan FDA registration 2f6edf9392b5544a879a5c8fdb4c00df
"BioSpeedia" Streptococcus Pneumoniae Kit (Non-Sterile)
TW: "拜歐速" 肺炎鏈球菌檢驗試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·BioSpeedia, SAS·Registered Jul 06, 2018 – Jul 06, 2023ExpiredRegistration details
- Analysis ID
- 2f6edf9392b5544a879a5c8fdb4c00df
- License Form
- Ministry of Health Medical Device Import No. 019279
- Customs Code
- DHA09401927906
Company information
- Manufacturer
- BioSpeedia, SAS
- Manufacturer Country
- France
- Authorized Representative
- YOULUM BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3740 Streptococcus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 06, 2018
- Expiry Date
- Jul 06, 2023
About this record
Access comprehensive regulatory information for "BioSpeedia" Streptococcus Pneumoniae 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 2f6edf9392b5544a879a5c8fdb4c00df and manufactured by BioSpeedia, SAS. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..
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