Taiwan FDA registration 85c6b9170806d6d7085a946ae88751ea
"ACRO" Clostridium difficile test kit (Non-Sterile)
TW: "艾快露" 困難梭狀芽胞桿菌檢驗試劑組 (未滅菌)
Registration details
- Analysis ID
- 85c6b9170806d6d7085a946ae88751ea
- License Form
- Ministry of Health Medical Device Import No. 017990
- Customs Code
- DHA09401799002
Company information
- Manufacturer
- ACRO BIOTECH. INC.
- Manufacturer Country
- United States
- Authorized Representative
- Grand Marquis IVD CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2660 Microbial identification and assay equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 19, 2017
- Expiry Date
- Jun 19, 2022
About this record
Access comprehensive regulatory information for "ACRO" Clostridium difficile test 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 85c6b9170806d6d7085a946ae88751ea and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..
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