Pure Global

"Americo" type A streptococcal reagent (unsterilized) - Taiwan Registration 286f62691a3820adf9e43e60983e9c6e

Access comprehensive regulatory information for "Americo" type A streptococcal reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 286f62691a3820adf9e43e60983e9c6e and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS 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 Database
Powered by Pure Global AI
89,000+ Devices
286f62691a3820adf9e43e60983e9c6e
Registration Details
Taiwan FDA Registration: 286f62691a3820adf9e43e60983e9c6e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Americo" type A streptococcal reagent (unsterilized)
TW: "ไบž็พŽๅˆฉๅฏ" Aๅž‹้ˆ็ƒ่Œ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

286f62691a3820adf9e43e60983e9c6e

DHA04600145302

Company Information

China

Product Details

Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).

C Immunology and microbiology

C.3740 ้ˆ็ƒ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

Input;; Chinese goods

Dates and Status

Aug 30, 2011

Aug 30, 2021

Oct 12, 2023

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€