Taiwan FDA registration 767c2577887cac6fb43b184c38293b6e

"Xiec" Human Bud Cystis Reagent Set (Unsterilized)

TW: "協克" 人芽囊原蟲試劑組 (未滅菌)

Taiwan·Risk Class 1·SAVYON DIAGNOSTICS LTD.·Registered Aug 10, 2011 – Aug 10, 2016Cancelled

Registration details

Analysis ID: 767c2577887cac6fb43b184c38293b6e
Customs Code: DHA04401068900

Company information

Manufacturer: SAVYON DIAGNOSTICS LTD.
Manufacturer Country: Israel
Authorized Representative: SEEKERS BIOMEDICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of "Histolytic amoeba serum reagent (C.3220)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3220 痢疾阿米巴血清試劑
Import Information: import

Dates and status

Registration Date: Aug 10, 2011
Expiry Date: Aug 10, 2016
Cancellation Date: May 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Xiec" Human Bud Cystis Reagent Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 767c2577887cac6fb43b184c38293b6e and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..

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