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"Ames" Monek suspension surgical system - Taiwan Registration 677134f9a4235b5a890ad22e8152d976

Access comprehensive regulatory information for "Ames" Monek suspension surgical system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 677134f9a4235b5a890ad22e8152d976 and manufactured by AMS Medical Systems Ireland Limited. The authorized representative in Taiwan is KUANPIRE ENTERPRISES CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AMERICAN MEDICAL SYSTEMS, and 1 recent registrations in the same category. 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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677134f9a4235b5a890ad22e8152d976
Registration Details
Taiwan FDA Registration: 677134f9a4235b5a890ad22e8152d976
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Device Details

"Ames" Monek suspension surgical system
TW: โ€œ่‰พๆข…ๆ–ฏโ€่Žซๅ…งๅ…‹ๆ‡ธๅŠๆ‰‹่ก“็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

677134f9a4235b5a890ad22e8152d976

DHA00602127302

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

Jul 26, 2010

Jul 26, 2020

Sep 19, 2018

Cancellation Information

Logged out

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