Taiwan FDA registration 9f9822619e5a77c25037f8db7d7a21e2

"WISH IN " H.pylori test (Non-Sterile)

TW: "微栩" 幽門螺旋桿菌檢驗試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·KAMIYA BIOMEDICAL COMPANY·Registered May 24, 2019 – May 24, 2024Expired
Registration details
Analysis ID
9f9822619e5a77c25037f8db7d7a21e2
License Form
Ministry of Health Medical Device Import No. 020482
Customs Code
DHA09402048203
Company information
Manufacturer Country
United States
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 devices
Product Type (Level 2)
C0003 Helicobacter serological reagent
Import Information
Imported from abroad
Dates and status
Registration Date
May 24, 2019
Expiry Date
May 24, 2024
About this record

Access comprehensive regulatory information for "WISH IN " H.pylori 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 9f9822619e5a77c25037f8db7d7a21e2 and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is WISH IN COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices