"Leishi" oxygen concentrator
Taiwan·Risk Class 2·Respironics, Inc.·Registered Aug 30, 2012 – Aug 30, 2027Active- Analysis ID
- b32994950c549d8e713f70c0b5a0cf5e
- Customs Code
- DHA00602394506
- Manufacturer
- Respironics, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- 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
- Registration Date
- Aug 30, 2012
- Expiry Date
- Aug 30, 2027
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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 b32994950c549d8e713f70c0b5a0cf5e and manufactured by 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., Flextronics Manufacturing Juarez 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.