Taiwan FDA registration 5ac273ec228fa150946efa9b07019d59

"ACRO" Mycoplasma Pneumoniae Test (Non-sterile)

TW: "愛可羅" 肺炎黴漿菌檢測試劑 (未滅菌)

Taiwan·Risk Class 1·MD·ACRO BIOTECH. INC.·Registered Jan 10, 2017 – Jan 10, 2027Active

Registration details

Analysis ID: 5ac273ec228fa150946efa9b07019d59
License Form: Ministry of Health Medical Device Import No. 017392
Customs Code: DHA09401739205

Company information

Manufacturer: ACRO BIOTECH. INC.
Manufacturer Country: United States
Authorized Representative: APPLIED BIOTECH ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3375 Mycoplasma serum reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 10, 2017
Expiry Date: Jan 10, 2027

About this record

Access comprehensive regulatory information for "ACRO" Mycoplasma Pneumoniae 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 5ac273ec228fa150946efa9b07019d59 and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..

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