"Leishi" oxygen concentrator
Taiwan·Risk Class 2·RESPIRONICS INC.;; Respironics, Inc.·Registered Dec 28, 2016 – Dec 28, 2026Active- Analysis ID
- 35df12a10e3621cd92c90f3c503d6795
- Customs Code
- DHA05602925902
- Manufacturer
- RESPIRONICS INC.;; 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
- Dec 28, 2016
- Expiry Date
- Dec 28, 2026
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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 35df12a10e3621cd92c90f3c503d6795 and manufactured by RESPIRONICS INC.;; 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 Flextronics Manufacturing Juarez 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.