Pure Global

Respitronics Elite Nebulization Therapy System - Taiwan Registration 8aa05b75cc97b4d662711d581ebcf481

Access comprehensive regulatory information for Respitronics Elite Nebulization Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8aa05b75cc97b4d662711d581ebcf481 and manufactured by PU YUAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PU YUAN BIOTECH 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
8aa05b75cc97b4d662711d581ebcf481
Registration Details
Taiwan FDA Registration: 8aa05b75cc97b4d662711d581ebcf481
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Respitronics Elite Nebulization Therapy System
TW: ไพๅŠ›็‰น้œงๅŒ–ๆฒป็™‚็ณป็ตฑ
Risk Class 2
MD

Registration Details

8aa05b75cc97b4d662711d581ebcf481

Ministry of Health Medical Device Manufacturing No. 007311

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

D Devices for anesthesiology

D5630 Sprayer

Produced in Taiwan, China

Dates and Status

Oct 07, 2021

Oct 07, 2026