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"Ames" light mesh prolapse repair system - Taiwan Registration ec5da38766204d9c264178fddb056bde

Access comprehensive regulatory information for "Ames" light mesh 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 ec5da38766204d9c264178fddb056bde and manufactured by AMS Medical Systems Ireland Limited. The authorized representative in Taiwan is KUANPIRE ENTERPRISES CORPORATION.

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ec5da38766204d9c264178fddb056bde
Registration Details
Taiwan FDA Registration: ec5da38766204d9c264178fddb056bde
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Device Details

"Ames" light mesh prolapse repair system
TW: โ€œ่‰พๆข…ๆ–ฏโ€้˜ฟๅšๅฅ‡่ผ•็ถฒ่„ซๅž‚ไฟฎ่ฃœ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

ec5da38766204d9c264178fddb056bde

DHA00601920401

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

Sep 08, 2008

Sep 08, 2018

Jun 07, 2022

Cancellation Information

Logged out

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