Taiwan FDA registration d09bcb19f8853baab9d96d3e752ccd46
"Leishi" bronchial examination elbow
TW: “磊仕”支氣管檢查彎管
Taiwan·Risk Class 2·RESPIRONICS INC.·Registered Oct 17, 2012 – Oct 17, 2027ActiveRegistration details
- Analysis ID
- d09bcb19f8853baab9d96d3e752ccd46
- Customs Code
- DHA00602413706
Company information
- Manufacturer
- RESPIRONICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- 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
Dates and status
- Registration Date
- Oct 17, 2012
- Expiry Date
- Oct 17, 2027
About this record
Access comprehensive regulatory information for "Leishi" bronchial examination elbow in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d09bcb19f8853baab9d96d3e752ccd46 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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