Taiwan FDA registration a9caffc547ca61874f898973789c64a6
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 Apr 25, 2023 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- a9caffc547ca61874f898973789c64a6
- License Form
- Ministry of Health Medical Device Import Registration No. a00170
- Customs Code
- DHA084a0017009
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 range of the "Non-powered Treatment Mattress (J.5150)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5150 Non-powered treatment mattress
Dates and status
- Registration Date
- Apr 25, 2023
- Expiry Date
- Oct 31, 2024
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 a9caffc547ca61874f898973789c64a6 and manufactured by Artilat NV. The authorized representative in Taiwan is EVERCARE MEDICAL INSTRUMENTS CO., LTD..
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