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"Squip" Ear, nose, and throat manual surgical instrument (Non-sterile) - Taiwan Registration 0cb9a16a2e458e7a2a859ecd52389c05

Access comprehensive regulatory information for "Squip" Ear, nose, and throat manual surgical instrument (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 0cb9a16a2e458e7a2a859ecd52389c05 and manufactured by SQUIP, INC.. The authorized representative in Taiwan is ANGEL MEDICAL INSTRUMENT 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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0cb9a16a2e458e7a2a859ecd52389c05
Registration Details
Taiwan FDA Registration: 0cb9a16a2e458e7a2a859ecd52389c05
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Device Details

"Squip" Ear, nose, and throat manual surgical instrument (Non-sterile)
TW: "้ฉ็‘ฐๅฏถ"่€ณ้ผปๅ–‰ๆ‰‹ๅ‹•ๅผๅค–็ง‘ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

0cb9a16a2e458e7a2a859ecd52389c05

Ministry of Health Medical Device Import No. 014832

DHA09401483205

Company Information

United States

Product Details

G ENT device

G4420 OTOLARYNGARY Manual Surgical Instrument

Imported from abroad

Dates and Status

Jan 09, 2015

Jan 09, 2020

Jun 16, 2022

Cancellation Information

Logged out

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