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"Quirses" clarifies the compress - Taiwan Registration cb32c061a397e98a3a70e684e8383f8e

Access comprehensive regulatory information for "Quirses" clarifies the compress in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb32c061a397e98a3a70e684e8383f8e and manufactured by TearScience, Inc.;; Remington Medical, S.A.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Remington Medical, Inc.;; TearScience, Inc., and 1 recent registrations in the same category. 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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cb32c061a397e98a3a70e684e8383f8e
Registration Details
Taiwan FDA Registration: cb32c061a397e98a3a70e684e8383f8e
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Device Details

"Quirses" clarifies the compress
TW: โ€œ้กŒ็ˆพ่ณฝๆ–ฏโ€ๆ˜Žๆ™ฐ็†ฑๆ•ทๅ™จ
Risk Class 2

Registration Details

cb32c061a397e98a3a70e684e8383f8e

DHA05603595301

Company Information

Dominican Republic;;United States

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M.5200 Eyelid Thermal Vibration System

Input;; Contract manufacturing

Dates and Status

Sep 25, 2022

Sep 25, 2027

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