Taiwan FDA registration a5049ff84eb6048d96006d09ae4901d0
"PARAMOUNT" Alternating pressure air flotation mattress (Non-Sterile)
TW: "派樂夢" 交替式壓力氣墊床 (未滅菌)
Taiwan·Risk Class 1·MD·PARAMOUNT BED CO., LTD. CHIBA FACTORY·Registered Jul 31, 2017 – Jul 31, 2022ExpiredRegistration details
- Analysis ID
- a5049ff84eb6048d96006d09ae4901d0
- License Form
- Ministry of Health Medical Device Import No. 018133
- Customs Code
- DHA09401813302
Company information
- Manufacturer
- PARAMOUNT BED CO., LTD. CHIBA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- SYM-MED ENTERPRISE CO., LTD
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5550 Alternating pressure air mattress
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 31, 2017
- Expiry Date
- Jul 31, 2022
About this record
Access comprehensive regulatory information for "PARAMOUNT" Alternating pressure air flotation 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 a5049ff84eb6048d96006d09ae4901d0 and manufactured by PARAMOUNT BED CO., LTD. CHIBA FACTORY. The authorized representative in Taiwan is SYM-MED ENTERPRISE CO., LTD.
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