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"Aixikang" excellent complete hernia system - Taiwan Registration 227b384752b3d1db3cdefec19c0fe0be

Access comprehensive regulatory information for "Aixikang" excellent complete hernia system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 227b384752b3d1db3cdefec19c0fe0be and manufactured by JOHNSON & JOHNSON MEDICAL GMBH;; Johnson & Johnson International, c/o European Logistics Centre. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL 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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227b384752b3d1db3cdefec19c0fe0be
Registration Details
Taiwan FDA Registration: 227b384752b3d1db3cdefec19c0fe0be
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Device Details

"Aixikang" excellent complete hernia system
TW: "ๆ„›ๆƒœๅบท"ๅ„ชๅ…จ่ฃœ็–ๆฐฃ็ณป็ตฑ
Risk Class 2

Registration Details

227b384752b3d1db3cdefec19c0fe0be

DHA00601769701

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

I.3300 Surgical mesh

import

Dates and Status

Jan 17, 2007

Jan 17, 2027