Taiwan FDA registration 4503b90823ba58ed6a4000d8c873c2c4

"Leishi" dream gel mask

TW: “磊仕”助夢凝膠面罩
Taiwan flagTaiwan·Risk Class 2·Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.·Registered Sep 08, 2017 – Sep 08, 2027Active
Registration details
Analysis ID
4503b90823ba58ed6a4000d8c873c2c4
Customs Code
DHA09200087000
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
Sep 08, 2017
Expiry Date
Sep 08, 2027
About this record

Access comprehensive regulatory information for "Leishi" dream gel mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4503b90823ba58ed6a4000d8c873c2c4 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 DatabasePowered by Pure Global AI89,000+ Devices