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OKcare Multi-Frequency Therapy Device - Taiwan Registration 8a95c9d53c136d40440a78d779cc6d27

Access comprehensive regulatory information for OKcare Multi-Frequency Therapy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8a95c9d53c136d40440a78d779cc6d27 and manufactured by OK BIOTECH CO., LTD.. The authorized representative in Taiwan is OK BIOTECH 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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8a95c9d53c136d40440a78d779cc6d27
Registration Details
Taiwan FDA Registration: 8a95c9d53c136d40440a78d779cc6d27
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Device Details

OKcare Multi-Frequency Therapy Device
TW: ๆญๅ…‹้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2
MD

Registration Details

8a95c9d53c136d40440a78d779cc6d27

Ministry of Health Medical Device Manufacturing No. 007077

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

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Produced in Taiwan, China

Dates and Status

Mar 02, 2021

Mar 02, 2026