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"Avis" Hengjie deproteinized oxygen system - Taiwan Registration 5132a7a0dfb5cb171e4df7bdfe3571e7

Access comprehensive regulatory information for "Avis" Hengjie deproteinized oxygen system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5132a7a0dfb5cb171e4df7bdfe3571e7 and manufactured by AVIZOR S.A.. The authorized representative in Taiwan is JI CHANG ENTERPRISE CO..

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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5132a7a0dfb5cb171e4df7bdfe3571e7
Registration Details
Taiwan FDA Registration: 5132a7a0dfb5cb171e4df7bdfe3571e7
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Device Details

"Avis" Hengjie deproteinized oxygen system
TW: "ๆ„›ๅ‰่ฆ–" ๆ†ๆฝ”ๅŽป่›‹็™ฝ้›™ๆฐง็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

5132a7a0dfb5cb171e4df7bdfe3571e7

DHA00601753807

Company Information

Spain

Product Details

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

M Ophthalmology

M.5918 Rigid Breathable Contact Lens Preservation Products

import

Dates and Status

Sep 27, 2006

Sep 27, 2011

Nov 26, 2012

Cancellation Information

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