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"MEDEPOT" Alternating Pressure Air Flotation Mattress (Non-Sterile) - Taiwan Registration f200d4f60dad6ce54a984263bf501776

Access comprehensive regulatory information for "MEDEPOT" 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 f200d4f60dad6ce54a984263bf501776 and manufactured by Changyi Precision Industry Co., Ltd. precision factory. The authorized representative in Taiwan is MEDEPOT CO., LTD.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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f200d4f60dad6ce54a984263bf501776
Registration Details
Taiwan FDA Registration: f200d4f60dad6ce54a984263bf501776
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Device Details

"MEDEPOT" Alternating Pressure Air Flotation Mattress (Non-Sterile)
TW: "็พŽ่ฟชๅฏถ" ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f200d4f60dad6ce54a984263bf501776

Ministry of Health Medical Device Manufacturing No. 007093

Company Information

Taiwan, Province of China

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

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Jan 24, 2018

Jan 24, 2023