Taiwan FDA registration 39a6b0ec37be77d2970536e276a656d8

"ALIFAX" Microtiter diluting and dispensing device (Non-sterile)

TW: "艾利福斯" 微滴定稀釋及分配器材 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Alifax S.r.l.·Registered Apr 10, 2019 – Apr 10, 2024Expired
Registration details
Analysis ID
39a6b0ec37be77d2970536e276a656d8
License Form
Ministry of Health Medical Device Import No. 020289
Customs Code
DHA09402028909
Company information
Manufacturer
Alifax S.r.l.
Manufacturer Country
Italy
Authorized Representative
GRAND MARQUIS CO., LTD.
Product details
Intended Use
Limited to the first level identification range of microtitration dilution and dispensing equipment (C.2500) of the management measures for medical devices.
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C2500 Microtitration Dilution and Dispensing Equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 10, 2019
Expiry Date
Apr 10, 2024
About this record

Access comprehensive regulatory information for "ALIFAX" Microtiter diluting and dispensing device (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 39a6b0ec37be77d2970536e276a656d8 and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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