Taiwan FDA registration 5ea43afcd9eecdd537d791ae60c0a764

"Micronylcan" pylori antigen test reagent (unsterilized)

TW: “微栩”幽門桿菌抗原檢驗試劑(未滅菌)
Taiwan flagTaiwan·Risk Class 1·WUHAN JIN PU MAN BIOTECH CO., LTD·Registered Sep 19, 2017 – Sep 19, 2022Cancelled
Registration details
Analysis ID
5ea43afcd9eecdd537d791ae60c0a764
Customs Code
DHA09600321907
Company information
Manufacturer Country
China
Authorized Representative
WISH IN COMPANY LIMITED
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.0003 螺旋桿菌屬血清試劑
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Sep 19, 2017
Expiry Date
Sep 19, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Micronylcan" pylori antigen 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 5ea43afcd9eecdd537d791ae60c0a764 and manufactured by WUHAN JIN PU MAN BIOTECH CO., LTD. The authorized representative in Taiwan is WISH IN COMPANY LIMITED.

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