"Leishi" sputum coughing auxiliary equipment
Taiwan·Risk Class 2·Respironics, Inc.·Registered Mar 05, 2013 – Mar 05, 2028Active- Analysis ID
- a626ef09c62161ff8e0ab026ef625190
- Customs Code
- DHA00602449009
- 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
- Mar 05, 2013
- Expiry Date
- Mar 05, 2028
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Access comprehensive regulatory information for "Leishi" sputum coughing auxiliary equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a626ef09c62161ff8e0ab026ef625190 and manufactured by Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESPIRONICS INC., and 1 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.