Taiwan FDA registration d3bb73c1ff07b14caf5a4a61c14d277f
“MORRIS” Therapeutic Humidifier for home use(NON-STERILE)
TW: “正氧”家用治療潮濕器(未滅菌)
Taiwan·Risk Class 1·MD·Oxygen Precision Technology Co., Ltd. Tainan Factory·Registered May 02, 2019 – May 02, 2024ExpiredRegistration details
- Analysis ID
- d3bb73c1ff07b14caf5a4a61c14d277f
- License Form
- Ministry of Health Medical Device Manufacturing No. 007742
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Oxygen Precision Technology Co., Ltd. Tainan Factory
Product details
- Intended Use
- Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Household Treatment Moisturizer (D.5460)".
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5460 Household Therapeutic Moisturizer
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 02, 2019
- Expiry Date
- May 02, 2024
About this record
Access comprehensive regulatory information for “MORRIS” Therapeutic Humidifier for home use(NON-STERILE) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d3bb73c1ff07b14caf5a4a61c14d277f and manufactured by Oxygen Precision Technology Co., Ltd. Tainan Factory. The authorized representative in Taiwan is Oxygen Precision Technology Co., Ltd. Tainan Factory.
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