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"Medi" Ruibang hernia repair net - Taiwan Registration cc42bdf87bb557de81224e7fa57edc57

Access comprehensive regulatory information for "Medi" Ruibang hernia repair net in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc42bdf87bb557de81224e7fa57edc57 and manufactured by MINNESOTA MEDICAL DEVELOPMENT, INC.. The authorized representative in Taiwan is Chengyi Limited.

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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cc42bdf87bb557de81224e7fa57edc57
Registration Details
Taiwan FDA Registration: cc42bdf87bb557de81224e7fa57edc57
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Device Details

"Medi" Ruibang hernia repair net
TW: โ€œ็พŽ่ฟชโ€็‘ž้‚ฆ็–ๆฐฃไฟฎ่ฃœ็ถฒ
Risk Class 2
Cancelled

Registration Details

cc42bdf87bb557de81224e7fa57edc57

DHA00602213008

Company Information

United States

Product Details

This product is used to assist in hernia repair and reinforcement or other soft tissue defects that can be supported with non-absorbable materials.

I General, Plastic Surgery and Dermatology

I.3300 Surgical mesh

import

Dates and Status

Mar 17, 2011

Mar 17, 2016

Aug 13, 2018

Cancellation Information

Logged out

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