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"PARAMOUNT" Alternating pressure air flotation mattress (Non-Sterile) - Taiwan Registration a5049ff84eb6048d96006d09ae4901d0

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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a5049ff84eb6048d96006d09ae4901d0
Registration Details
Taiwan FDA Registration: a5049ff84eb6048d96006d09ae4901d0
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Device Details

"PARAMOUNT" Alternating pressure air flotation mattress (Non-Sterile)
TW: "ๆดพๆจ‚ๅคข" ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a5049ff84eb6048d96006d09ae4901d0

Ministry of Health Medical Device Import No. 018133

DHA09401813302

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".

J General hospital and personal use equipment

J5550 Alternating pressure air mattress

Imported from abroad

Dates and Status

Jul 31, 2017

Jul 31, 2022