"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.
Device Details
Registration Details
0cb9a16a2e458e7a2a859ecd52389c05
Ministry of Health Medical Device Import No. 014832
DHA09401483205
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
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