Taiwan FDA registration 67095a9ba75448e10ff271d8cd3199c2

"Leishi" Iver mouth and nose mask

TW: “磊仕”艾弗口鼻面罩
Taiwan flagTaiwan·Risk Class 2·Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.·Registered Oct 27, 2017 – Oct 27, 2027Active
Registration details
Analysis ID
67095a9ba75448e10ff271d8cd3199c2
Customs Code
DHA09200087701
Company information
Manufacturer Country
United States;;China
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5905 Non-continuous respirators
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Oct 27, 2017
Expiry Date
Oct 27, 2027
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About this record

Access comprehensive regulatory information for "Leishi" Iver mouth and nose mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67095a9ba75448e10ff271d8cd3199c2 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, 1 companies making similar products including Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd., and 1 recent registrations in the same category. 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.

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