"Lei" oxygen concentrator
Taiwan·Risk Class 2·RESPIRONICS GEORGIA, INC.·Registered Sep 04, 2006 – Sep 04, 2011Cancelled- Analysis ID
- b6faa77ebd91092f68e5db6fc294ba30
- Customs Code
- DHA00601707506
- Manufacturer
- RESPIRONICS GEORGIA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ASIAMED INSTRUMENTS CO., LTD.
- Intended Use
- Supplemental oxygen is provided to patients who require low-flow oxygen therapy.
- Product Type (Level 1)
- D Anesthesiology
- Import Information
- import
- Registration Date
- Sep 04, 2006
- Expiry Date
- Sep 04, 2011
- Cancellation Date
- Nov 30, 2012
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 b6faa77ebd91092f68e5db6fc294ba30 and manufactured by RESPIRONICS GEORGIA, 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 Flextronics Manufacturing Juárez S. de R.L. de C.V.; 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.