Taiwan FDA registration 99f454c0b453a6e0d8314fbda0939d39
"Leishi" Yimei disposable full face mask
TW: “磊仕”依美拋棄式全面罩
Taiwan·Risk Class 2·RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SHENZHEN) CO., LTD.·Registered Mar 23, 2012 – Mar 23, 2017CancelledRegistration details
- Analysis ID
- 99f454c0b453a6e0d8314fbda0939d39
- Customs Code
- DHA04200033100
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
- import
Dates and status
- Registration Date
- Mar 23, 2012
- Expiry Date
- Mar 23, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Leishi" Yimei disposable full face mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 99f454c0b453a6e0d8314fbda0939d39 and manufactured by RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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