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"Bonte" ureteral catheter group - Taiwan Registration 7c5f2e594c895e84fc8c1e3ad8efd1b5

Access comprehensive regulatory information for "Bonte" ureteral catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7c5f2e594c895e84fc8c1e3ad8efd1b5 and manufactured by Bangte Biotechnology Co., Ltd. Yike Factory. The authorized representative in Taiwan is BIOTEQUE CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Bonte Biotechnology Co., Ltd. Yilan Plant 2, 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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7c5f2e594c895e84fc8c1e3ad8efd1b5
Registration Details
Taiwan FDA Registration: 7c5f2e594c895e84fc8c1e3ad8efd1b5
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Device Details

"Bonte" ureteral catheter group
TW: โ€œ้‚ฆ็‰นโ€่ผธๅฐฟ็ฎกๅฐŽ็ฎก็ต„
Risk Class 2

Registration Details

7c5f2e594c895e84fc8c1e3ad8efd1b5

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.4620 Urinary Catheter Stent

Domestic

Dates and Status

Nov 08, 2024

Nov 08, 2029

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