Taiwan FDA registration 1f168ba253e1c5bd4f485e107e3e1310
“Artilat”Nonpowered flotation therapy mattress (Non-Sterile)
TW: “愛迪麗特”非動力式治療床墊(未滅菌)
Taiwan·Risk Class 1·MD·ARTILAT NV·Registered Oct 01, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 1f168ba253e1c5bd4f485e107e3e1310
- License Form
- Ministry of Health Medical Device Import Registration No. 012811
- Customs Code
- DHA08401281104
Company information
- Manufacturer
- ARTILAT NV
- Manufacturer Country
- Belgium
- Authorized Representative
- EVERCARE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5150 Non-powered treatment mattress
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for “Artilat”Nonpowered flotation therapy mattress (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 1f168ba253e1c5bd4f485e107e3e1310 and manufactured by ARTILAT NV. The authorized representative in Taiwan is EVERCARE MEDICAL INSTRUMENTS CO., LTD..
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