Taiwan FDA registration d5afa91f6448c3b7bd6f1aa95e3406a1
"Leishi" humid heater
TW: "磊仕"潮濕加熱器
Taiwan·Risk Class 2·RESPIRONICS INC.;; Respironics, Inc.·Registered May 12, 2016 – May 12, 2026ExpiredRegistration details
- Analysis ID
- d5afa91f6448c3b7bd6f1aa95e3406a1
- Customs Code
- DHA05602853301
Company information
- Manufacturer
- RESPIRONICS INC.;; 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.5450 Vapor moisture apparatus for respirators
- Import Information
- import
Dates and status
- Registration Date
- May 12, 2016
- Expiry Date
- May 12, 2026
About this record
Access comprehensive regulatory information for "Leishi" humid heater in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5afa91f6448c3b7bd6f1aa95e3406a1 and manufactured by RESPIRONICS INC.;; Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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