Pure Global

Mei Ariel Nyazi Parasite Test Kit (Unsterilized) - Taiwan Registration 583ef3bcd613a1829f444c150e891b8a

Access comprehensive regulatory information for Mei Ariel Nyazi Parasite Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 583ef3bcd613a1829f444c150e891b8a and manufactured by ALERE SAN DIEGO, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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 Database
Powered by Pure Global AI
89,000+ Devices
583ef3bcd613a1829f444c150e891b8a
Registration Details
Taiwan FDA Registration: 583ef3bcd613a1829f444c150e891b8a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Mei Ariel Nyazi Parasite Test Kit (Unsterilized)
TW: ็พŽ่‰พๅˆฉ็ˆพ ๆฃ่€ถๆฟŸ ๅฏ„็”Ÿ่Ÿฒๆชขๆธฌๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

583ef3bcd613a1829f444c150e891b8a

DHA04400965904

Company Information

United States

Product Details

Limited to the first level identification range of "Histolytic amoeba serum reagent (C.3220)" of the Measures for the Administration of Medical Devices.

C Immunology and microbiology

C.3220 ็—ข็–พ้˜ฟ็ฑณๅทด่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 10, 2010

Dec 10, 2020

Jul 15, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€