Taiwan FDA registration 81a186cb52ef23dc5f056bd370486647

"Lei" oxygen concentrator

TW: “磊士”氧氣濃縮機
Taiwan flagTaiwan·Risk Class 2·RESPIRONICS INC.·Registered Jun 02, 2008 – Jun 02, 2013Cancelled
Registration details
Analysis ID
81a186cb52ef23dc5f056bd370486647
Customs Code
DHA00601888201
Company information
Manufacturer
RESPIRONICS INC.
Manufacturer Country
United States
Authorized Representative
ASIAMED INSTRUMENTS CO., LTD.
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
Jun 02, 2008
Expiry Date
Jun 02, 2013
Cancellation Date
Aug 04, 2015
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 81a186cb52ef23dc5f056bd370486647 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is ASIAMED INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including RESPIRONICS GEORGIA, INC., Flextronics Manufacturing Juárez S. de R.L. de C.V.; 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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