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"Aixikan" Beroren hernia system with non-absorbable mesh - Taiwan Registration 1fb6255ce3e6608852f0ff9f302202c0

Access comprehensive regulatory information for "Aixikan" Beroren hernia system with non-absorbable mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fb6255ce3e6608852f0ff9f302202c0 and manufactured by ETHICON INC.. 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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1fb6255ce3e6608852f0ff9f302202c0
Registration Details
Taiwan FDA Registration: 1fb6255ce3e6608852f0ff9f302202c0
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Device Details

"Aixikan" Beroren hernia system with non-absorbable mesh
TW: "ๆ„›ๆƒœๅบท" ไผฏ็พ…ๅ€ซ็–ๆฐฃ็ณป็ตฑ็”จไธๅฏๅธๆ”ถ็ถฒ
Risk Class 2
Cancelled

Registration Details

1fb6255ce3e6608852f0ff9f302202c0

DHA00600965107

Company Information

United States

Product Details

I000 General, Plastic Surgery and Dermatology

import

Dates and Status

Apr 25, 2001

Apr 25, 2026

Dec 09, 2021

Cancellation Information

Logged out

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