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"Ronamac" Antistammering device (Non-Sterile) - Taiwan Registration bb8adef291aec93668c99f6958dce14b

Access comprehensive regulatory information for "Ronamac" Antistammering device (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 bb8adef291aec93668c99f6958dce14b and manufactured by ARTICULATE INSTRUMENTS 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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Registration Details
Taiwan FDA Registration: bb8adef291aec93668c99f6958dce14b
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Device Details

"Ronamac" Antistammering device (Non-Sterile)
TW: "ๆœ‹็ฌ›"ๅฃๅƒ็Ÿฏๆญฃๅ™จๆ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

bb8adef291aec93668c99f6958dce14b

Ministry of Health Medical Device Import No. 019419

DHA09401941909

Company Information

United Kingdom

Product Details

Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Stuttering Correction Equipment (G.5840)".

G ENT device

G5840 Stutter correction device

Imported from abroad

Dates and Status

Jul 26, 2018

Jul 26, 2023