Pure Global

"Leishi" Iver full mask - Taiwan Registration 13824f7487546f0ecc5f9eada040d183

Access comprehensive regulatory information for "Leishi" Iver full mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 13824f7487546f0ecc5f9eada040d183 and manufactured by Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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
13824f7487546f0ecc5f9eada040d183
Registration Details
Taiwan FDA Registration: 13824f7487546f0ecc5f9eada040d183
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Leishi" Iver full mask
TW: โ€œ็ฃŠไป•โ€่‰พๅผ—ๅ…จ้ข็ฝฉ
Risk Class 2
Cancelled

Registration Details

13824f7487546f0ecc5f9eada040d183

DHA04200033202

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5905 Non-continuous respirators

Input;; Contract manufacturing

Dates and Status

Mar 29, 2012

Mar 29, 2022

Apr 12, 2024

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ