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"Bard" Anjie adjustable single-cut suspension - Taiwan Registration 65ffb6c27d9263d5ab6397e288341e16

Access comprehensive regulatory information for "Bard" Anjie adjustable single-cut suspension in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 65ffb6c27d9263d5ab6397e288341e16 and manufactured by C.R. BARD, INC.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., 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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65ffb6c27d9263d5ab6397e288341e16
Registration Details
Taiwan FDA Registration: 65ffb6c27d9263d5ab6397e288341e16
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Device Details

"Bard" Anjie adjustable single-cut suspension
TW: โ€œๅทดๅพทโ€ๅฎ‰ๆฝ”่ชฟๆ•ดๅž‹ๅ–ฎๅˆ‡ๅฃๆ‡ธๅธถ
Risk Class 2
Cancelled

Registration Details

65ffb6c27d9263d5ab6397e288341e16

DHA00602241804

Company Information

United States

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

May 24, 2011

May 24, 2021

Sep 08, 2023

Cancellation Information

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