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"OKmeter"Hearing Aid (Non-Sterile) - Taiwan Registration 7a03f6d42b21f8abed3716b850726f14

Access comprehensive regulatory information for "OKmeter"Hearing Aid (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 7a03f6d42b21f8abed3716b850726f14 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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7a03f6d42b21f8abed3716b850726f14
Registration Details
Taiwan FDA Registration: 7a03f6d42b21f8abed3716b850726f14
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Device Details

"OKmeter"Hearing Aid (Non-Sterile)
TW: "ๆญๅ…‹"ๅŠฉ่ฝๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

7a03f6d42b21f8abed3716b850726f14

Ministry of Health Medical Device Manufacturing No. 008205

Company Information

Taiwan, Province of China

Product Details

G ENT device

G3300 hearing aid

Produced in Taiwan, China

Dates and Status

Feb 21, 2020

Feb 21, 2025

Jan 05, 2023