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"Ampli" hearing impaired tester and its accessories - Taiwan Registration f4fb39d5e70a212f65be3f8259c55e2b

Access comprehensive regulatory information for "Ampli" hearing impaired tester and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4fb39d5e70a212f65be3f8259c55e2b and manufactured by AMPLIVOX LTD.. The authorized representative in Taiwan is RONAMAC INTERNATIONAL CORP..

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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f4fb39d5e70a212f65be3f8259c55e2b
Registration Details
Taiwan FDA Registration: f4fb39d5e70a212f65be3f8259c55e2b
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Device Details

"Ampli" hearing impaired tester and its accessories
TW: โ€œๅฎ‰ๆ™ฎๅŠ›โ€่ฝ้˜ปๆชขๆŸฅๅ„€ๅŠๅ…ถ้…ไปถ
Risk Class 2
Cancelled

Registration Details

f4fb39d5e70a212f65be3f8259c55e2b

DHA00602371706

Company Information

United Kingdom

Product Details

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

G ENT Science

G.1090 Auditory Resistance Checker

import

Dates and Status

Jul 25, 2012

Jul 25, 2022

Apr 12, 2024

Cancellation Information

Logged out

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