Taiwan FDA registration 0343684958652fb048c54eec29a5fbab

"Ikrimicus" Klebsiella pneumoniae K1/K2 serotyping quick screening card (unsterilized)

TW: "碁米庫斯" 克雷伯氏肺炎桿菌K1/K2血清分型快篩卡(未滅菌)

Taiwan·Risk Class 1·FIRSTEP BIORESEARCH INC.·Registered Nov 13, 2017 – Nov 13, 2022Cancelled

Registration details

Analysis ID: 0343684958652fb048c54eec29a5fbab

Company information

Manufacturer: FIRSTEP BIORESEARCH INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: KEMYTH BIOTECH CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Administrative Measures for Medical Devices "Klebsiella serological reagent (C.3340)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3340 克雷白氏桿菌屬血清試劑
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Nov 13, 2017
Expiry Date: Nov 13, 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 "Ikrimicus" Klebsiella pneumoniae K1/K2 serotyping quick screening card (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0343684958652fb048c54eec29a5fbab and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is KEMYTH BIOTECH CO., LTD..

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