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"Bard" urethral dilator attachment (unsterilized) - Taiwan Registration 0330e94f1314e9dd89c610e489367c50

Access comprehensive regulatory information for "Bard" urethral dilator attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0330e94f1314e9dd89c610e489367c50 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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0330e94f1314e9dd89c610e489367c50
Registration Details
Taiwan FDA Registration: 0330e94f1314e9dd89c610e489367c50
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Device Details

"Bard" urethral dilator attachment (unsterilized)
TW: โ€œๅทดๅพทโ€ๅฐฟ้“ๆ“ดๅผตๅ™จ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0330e94f1314e9dd89c610e489367c50

DHA04400825300

Company Information

United States

Product Details

Limited to the first level identification range of "urethral dilator (H.5520)" of the Measures for the Administration of Medical Devices.

H Gastroenterology and urology

H.5520 Urethral extender

import

Dates and Status

Jan 08, 2010

Jan 08, 2015

May 28, 2018

Cancellation Information

Logged out

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