Taiwan FDA registration bf0ecd4d53f622806a4e664ac28e795f
"Leishi" physiological recorder
TW: “磊仕”生理記錄儀
Taiwan·Risk Class 2·Kimball Electronics Group LLC- Jasper;; RESPIRONICS INC.·Registered Oct 23, 2017 – Oct 23, 2027ActiveRegistration details
- Analysis ID
- bf0ecd4d53f622806a4e664ac28e795f
- Customs Code
- DHA05603036307
Company information
- 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.2375 Respiratory frequency monitor
- Import Information
- import
Dates and status
- Registration Date
- Oct 23, 2017
- Expiry Date
- Oct 23, 2027
About this record
Access comprehensive regulatory information for "Leishi" physiological recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf0ecd4d53f622806a4e664ac28e795f and manufactured by Kimball Electronics Group LLC- Jasper;; RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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