Taiwan FDA registration 13824f7487546f0ecc5f9eada040d183
"Leishi" Iver full mask
TW: “磊仕”艾弗全面罩
Taiwan·Risk Class 2·Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.·Registered Mar 29, 2012 – Mar 29, 2022CancelledRegistration details
- Analysis ID
- 13824f7487546f0ecc5f9eada040d183
- Customs Code
- DHA04200033202
Company information
- Manufacturer Country
- United States;;China
- 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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Mar 29, 2012
- Expiry Date
- Mar 29, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Leishi" Iver full mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 13824f7487546f0ecc5f9eada040d183 and manufactured by Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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