Taiwan FDA registration 7948b3030037f269fc11f66448b8fba0

"Lei" oxygen concentrator

TW: “磊士”氧氣濃縮機
Taiwan flagTaiwan·Risk Class 2·Flextronics Manufacturing Juárez S. de R.L. de C.V.; Respironics, Inc.·Registered Oct 18, 2007 – Oct 18, 2027Active
Registration details
Analysis ID
7948b3030037f269fc11f66448b8fba0
Customs Code
DHA00601836303
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
import
Dates and status
Registration Date
Oct 18, 2007
Expiry Date
Oct 18, 2027
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About this record

Access comprehensive regulatory information for "Lei" 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 7948b3030037f269fc11f66448b8fba0 and manufactured by Flextronics Manufacturing Juárez 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 GEORGIA, 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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