"Leishi" positive pressure respiratory system
Taiwan·Risk Class 2·RESPIRONICS INC.;; Respironics, Inc.·Registered Jan 08, 2016 – Jan 08, 2026Expired- Analysis ID
- edc45a83c5a6cb7664db63f92c93dbfa
- Customs Code
- DHA05602813900
- Manufacturer
- RESPIRONICS INC.;; Respironics, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- 'Respironics" DreamStation CPAP System
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5905 Non-continuous respirators
- Import Information
- import
- Registration Date
- Jan 08, 2016
- Expiry Date
- Jan 08, 2026
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Access comprehensive regulatory information for "Leishi" positive pressure respiratory system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number edc45a83c5a6cb7664db63f92c93dbfa 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 RESPIRONICS INC., RESPIRONICS INC.;; Respironics, Inc., and 5 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.