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"Ames" Alibet prolapse repair system - Taiwan Registration 4dc19696f85a7a492b5ab1dccf654cf3

Access comprehensive regulatory information for "Ames" Alibet prolapse repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dc19696f85a7a492b5ab1dccf654cf3 and manufactured by AMS Medical Systems Ireland Limited. The authorized representative in Taiwan is KUANPIRE ENTERPRISES CORPORATION.

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4dc19696f85a7a492b5ab1dccf654cf3
Registration Details
Taiwan FDA Registration: 4dc19696f85a7a492b5ab1dccf654cf3
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Device Details

"Ames" Alibet prolapse repair system
TW: โ€œ่‰พๆข…ๆ–ฏโ€ๆ„›ๅŠ›ๅ€็‰น่„ซๅž‚ไฟฎ่ฃœ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

4dc19696f85a7a492b5ab1dccf654cf3

DHA00602132900

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

Aug 25, 2010

Aug 25, 2020

Sep 19, 2018

Cancellation Information

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