"Leishi" positive pressure respiratory system
Taiwan·Risk Class 2·RESPIRONICS INC.·Registered Dec 05, 2012 – Dec 05, 2022Cancelled- Analysis ID
- 2f222a923ddf0ae280950950a0021421
- Customs Code
- DHA00602424407
- 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.5905 Non-continuous respirators
- Import Information
- import
- Registration Date
- Dec 05, 2012
- Expiry Date
- Dec 05, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 2f222a923ddf0ae280950950a0021421 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.;; 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.