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Gyn Glaucoma Treatment System - Taiwan Registration 1ee49a788267b407142ccfdd78ec6886

Access comprehensive regulatory information for Gyn Glaucoma Treatment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ee49a788267b407142ccfdd78ec6886 and manufactured by Trelleborg Sealing Solutions US, Inc.;; Allergan Sales, LLC. The authorized representative in Taiwan is ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND).

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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1ee49a788267b407142ccfdd78ec6886
Registration Details
Taiwan FDA Registration: 1ee49a788267b407142ccfdd78ec6886
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Device Details

Gyn Glaucoma Treatment System
TW: ๆทๆฉ้’ๅ…‰็œผๆฒป็™‚็ณป็ตฑ
Risk Class 2

Registration Details

1ee49a788267b407142ccfdd78ec6886

DHA05603009600

Product Details

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

M Ophthalmology

M.3920 Aqueous aqueous veil implants

Contract manufacturing;; input

Dates and Status

Jan 09, 2018

Jan 09, 2028