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"Ottobock" Flotation cushion (Non-Sterile) - Taiwan Registration 5b224539ea6244b80b0074abb6e33c85

Access comprehensive regulatory information for "Ottobock" Flotation cushion (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 5b224539ea6244b80b0074abb6e33c85 and manufactured by OTTOBOCK HEALTHCARE LP. The authorized representative in Taiwan is OTTO BOCK ASIA PACIFIC LIMITED TAIWAN BRANCH (H.K.).

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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5b224539ea6244b80b0074abb6e33c85
Registration Details
Taiwan FDA Registration: 5b224539ea6244b80b0074abb6e33c85
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Device Details

"Ottobock" Flotation cushion (Non-Sterile)
TW: "ๅฅงๆ‰˜ๅšๅ…‹" ๆธ›ๅฃ“ๅๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5b224539ea6244b80b0074abb6e33c85

Ministry of Health Medical Device Import No. 016509

DHA09401650908

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".

o Equipment for physical medicine

O3175 floating seat cushion

Imported from abroad

Dates and Status

May 10, 2016

May 10, 2026