"Leishi" sputum coughing auxiliary equipment
Taiwan·Risk Class 2·RESPIRONICS INC.·Registered Oct 17, 2011 – Oct 17, 2016Cancelled- Analysis ID
- 4ad698bdc52c74bde9fb31c563484996
- Customs Code
- DHA00602284204
- 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
- Oct 17, 2011
- Expiry Date
- Oct 17, 2016
- Cancellation Date
- Apr 25, 2018
- Status
- Logged out
- Reason
- 自行鍵入
Top companies providing products similar to ""Leishi" sputum coughing auxiliary equipment"
Recently registered similar products
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 4ad698bdc52c74bde9fb31c563484996 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.