Taiwan FDA registration 734c6e0dde715a1c9c830efa224ba4b0
"ACRO BIOTECH" Legionella-Ag test (Non-Sterile)
TW: "愛可羅" 退伍軍人肺炎抗原檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·ACRO BIOTECH INC.·Registered Apr 17, 2020 – Apr 17, 2025ExpiredRegistration details
- Analysis ID
- 734c6e0dde715a1c9c830efa224ba4b0
- License Form
- Ministry of Health Medical Device Import No. 021466
- Customs Code
- DHA09402146600
Company information
- Manufacturer
- ACRO BIOTECH INC.
- Manufacturer Country
- United States
- Authorized Representative
- APPLIED BIOTECH ENTERPRISE 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
- Apr 17, 2020
- Expiry Date
- Apr 17, 2025
About this record
Access comprehensive regulatory information for "ACRO BIOTECH" Legionella-Ag 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 734c6e0dde715a1c9c830efa224ba4b0 and manufactured by ACRO BIOTECH INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
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