Taiwan FDA registration cce9788ac20bd943d2f484560021846b

"Yida" Pylori Rapid Test Reagent (Unsterilized)

TW: "醫達" 幽門桿菌快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·TONYAR BIOTECH. INC.·Registered Sep 06, 2012 – Sep 06, 2017Cancelled

Registration details

Analysis ID: cce9788ac20bd943d2f484560021846b

Company information

Manufacturer: TONYAR BIOTECH. INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: E-TAKE TECHNOLOGY CO., LTD.

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: Contract manufacturing;; Domestic

Dates and status

Registration Date: Sep 06, 2012
Expiry Date: Sep 06, 2017
Cancellation Date: Aug 01, 2019

Cancellation information

Status: Logged out
Reason: 未展延而逾期者;;自請註銷

About this record

Access comprehensive regulatory information for "Yida" Pylori 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 cce9788ac20bd943d2f484560021846b and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is E-TAKE TECHNOLOGY CO., LTD..

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