Taiwan FDA registration 82d47c8acf2ed2cf468d633fea882267
"Siloam" Rotavirus/Adenovirus Combi-test (Non-Sterile)
TW: "西羅亞" 輪狀病毒/腺病毒二合一檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered Sep 09, 2016 – Sep 09, 2021ExpiredRegistration details
- Analysis ID
- 82d47c8acf2ed2cf468d633fea882267
- License Form
- Ministry of Health Medical Device Import No. 016986
- Customs Code
- DHA09401698603
Company information
- Manufacturer
- MD BIOTECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Siloam Biotech Co., Ltd.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3020 adenovirus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 09, 2016
- Expiry Date
- Sep 09, 2021
About this record
Access comprehensive regulatory information for "Siloam" Rotavirus/Adenovirus Combi-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 82d47c8acf2ed2cf468d633fea882267 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is Siloam Biotech Co., Ltd..
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