Taiwan FDA registration d3817474282e20e68456e9cfc61e4e70

"Leishi" oxygen concentrator

TW: “磊仕”氧氣濃縮機
Taiwan flagTaiwan·Risk Class 2·Flextronics Manufacturing Juarez S. de R.L. de C.V.;; RESPIRONICS INC.·Registered Jul 28, 2014 – Jul 28, 2029Active
Registration details
Analysis ID
d3817474282e20e68456e9cfc61e4e70
Customs Code
DHA05602641205
Company information
Manufacturer Country
Mexico;;United States
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.5440 Portable Oxygen Generator
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Jul 28, 2014
Expiry Date
Jul 28, 2029
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About this record

Access comprehensive regulatory information for "Leishi" oxygen concentrator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3817474282e20e68456e9cfc61e4e70 and manufactured by Flextronics Manufacturing Juarez S. de R.L. de C.V.;; RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including RESPIRONICS INC.;; Respironics, Inc., Respironics, Inc., and 2 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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