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ACUVUE OASYS MAX 1-DAY MULTIFOCAL - Taiwan Registration d2db48342ad406c80d7684170be2c556

Access comprehensive regulatory information for ACUVUE OASYS MAX 1-DAY MULTIFOCAL in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2db48342ad406c80d7684170be2c556 and manufactured by JOHNSON & JOHNSON VISION CARE, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON TAIWAN 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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d2db48342ad406c80d7684170be2c556
Registration Details
Taiwan FDA Registration: d2db48342ad406c80d7684170be2c556
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Device Details

ACUVUE OASYS MAX 1-DAY MULTIFOCAL
TW: ๅฎ‰่ฆ–ๅ„ชๆญ่ˆ’้ฉๆฅตๆฝคๅคš็„ฆ้ปž้ซ˜้€ๆฐง็Ÿฝๆฐด่† ๆฏๆ—ฅๆ‹‹
Risk Class 2
MD

Registration Details

d2db48342ad406c80d7684170be2c556

Ministry of Health Medical Device Import No. 036359

DHA05603635907

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M5925 Flexible Contact Lens

Imported from abroad

Dates and Status

May 10, 2023

May 10, 2028