Pure Global

"Firstep" Saliva Collection Kit (Non-Sterile) - Taiwan Registration 97ba48e748073233680fc9ff19534668

Access comprehensive regulatory information for "Firstep" Saliva Collection Kit (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 97ba48e748073233680fc9ff19534668 and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..

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
97ba48e748073233680fc9ff19534668
Registration Details
Taiwan FDA Registration: 97ba48e748073233680fc9ff19534668
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Firstep" Saliva Collection Kit (Non-Sterile)
TW: "่ฏ่ฏ" ๅ”พๆถฒๆŽก้›†็›’ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

97ba48e748073233680fc9ff19534668

Ministry of Health Medical Device Manufacturing No. 007345

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".

C Immunology and microbiology devices

C2900 Microbial sample collection and delivery device

Produced in Taiwan, China

Dates and Status

Jul 13, 2018

Jul 13, 2023