Taiwan FDA registration 387aca9f44a3887e45ceb32b65ea8a13

"Aikuailu" Vaginal pH Rapid Test Reagent (Unsterilized)

TW: "艾快露" 陰道酸鹼值快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·ACRO BIOTECH INC.·Registered Oct 13, 2016 – Oct 13, 2026Active

Registration details

Analysis ID: 387aca9f44a3887e45ceb32b65ea8a13
Customs Code: DHA09401707700

Company information

Manufacturer: ACRO BIOTECH INC.
Manufacturer Country: United States
Authorized Representative: Grand Marquis IVD CO., LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "Uric pH (Non-quantitative) Test System (A.1550)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1550 Uric pH (non-quantitative) testing system
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Oct 13, 2016
Expiry Date: Oct 13, 2026

About this record

Access comprehensive regulatory information for "Aikuailu" Vaginal pH Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 387aca9f44a3887e45ceb32b65ea8a13 and manufactured by ACRO BIOTECH INC.. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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