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SPIO Compression Orthosis (Non-Sterile) - Taiwan Registration f870f7e8b36f753d4afde55eacf7df4e

Access comprehensive regulatory information for SPIO Compression Orthosis (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 f870f7e8b36f753d4afde55eacf7df4e and manufactured by SPIO, Inc.. The authorized representative in Taiwan is Fuyu Medical Equipment 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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f870f7e8b36f753d4afde55eacf7df4e
Registration Details
Taiwan FDA Registration: f870f7e8b36f753d4afde55eacf7df4e
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Device Details

SPIO Compression Orthosis (Non-Sterile)
TW: ๆ–ฏๆฏ”ๆญๅขžๅฃ“็Ÿฏๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

f870f7e8b36f753d4afde55eacf7df4e

Ministry of Health Medical Device Import No. 019585

DHA09401958500

Company Information

United States

Product Details

o Equipment for physical medicine

O9999 Other

Imported from abroad

Dates and Status

Sep 07, 2018

Sep 07, 2023

Feb 18, 2022

Cancellation Information

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