Taiwan FDA registration 977ed0323dbec956d89a709ab7c3d205

"Savyon" Helicobacter pylori Antigen Rapid Test (Non-Sterile)

TW: "賽維翁" 幽門桿菌抗原快速檢測試劑(未滅菌)

Taiwan·Risk Class 1·MD·SAVYON DIAGNOSTICS LTD.·Registered Jan 30, 2018 – Jan 30, 2028Active

Registration details

Analysis ID: 977ed0323dbec956d89a709ab7c3d205
License Form: Ministry of Health Medical Device Import No. 018776
Customs Code: DHA09401877602

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 the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C0003 Helicobacter serological reagent
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 30, 2018
Expiry Date: Jan 30, 2028

About this record

Access comprehensive regulatory information for "Savyon" Helicobacter pylori Antigen Rapid Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 977ed0323dbec956d89a709ab7c3d205 and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..

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