Taiwan FDA registration 2da992d6c7686206b805009de35c7ad7
"Leishi" mask bend
TW: “磊仕”面罩彎管
Taiwan·Risk Class 2·RESPIRONICS INC.·Registered Aug 22, 2012 – Aug 22, 2027ActiveRegistration details
- Analysis ID
- 2da992d6c7686206b805009de35c7ad7
- Customs Code
- DHA00602393901
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
- Aug 22, 2012
- Expiry Date
- Aug 22, 2027
About this record
Access comprehensive regulatory information for "Leishi" mask bend in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2da992d6c7686206b805009de35c7ad7 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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