Taiwan FDA registration 9948a02cd6dc19d919f0ecd72687a36a
Hao Di ultraviolet sterilization light sterilizer
TW: 濠笛紫外線除菌光殺菌器
Taiwan·Risk Class 2·EZ MEDICA CO., LTD.·Registered Jun 19, 2012 – Jun 19, 2017CancelledRegistration details
- Analysis ID
- 9948a02cd6dc19d919f0ecd72687a36a
Company information
- Manufacturer
- EZ MEDICA CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Furen Enterprises Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6500 Medical UV Air Purifier
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jun 19, 2012
- Expiry Date
- Jun 19, 2017
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Hao Di ultraviolet sterilization light sterilizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9948a02cd6dc19d919f0ecd72687a36a and manufactured by EZ MEDICA CO., LTD.. The authorized representative in Taiwan is Furen Enterprises Limited.
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