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"Berty" Central Venous Catheter Group - Taiwan Registration 36948eb1ec57ea795e2d80a23066232a

Access comprehensive regulatory information for "Berty" Central Venous 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 36948eb1ec57ea795e2d80a23066232a and manufactured by Bioptimal International Pte. Ltd.. The authorized representative in Taiwan is HSIN TUNG MEDICAL 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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36948eb1ec57ea795e2d80a23066232a
Registration Details
Taiwan FDA Registration: 36948eb1ec57ea795e2d80a23066232a
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Device Details

"Berty" Central Venous Catheter Group
TW: โ€œๆŸ่’‚โ€ ไธญๅคฎ้œ่„ˆๅฐŽ็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

36948eb1ec57ea795e2d80a23066232a

DHA00602290301

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

J.5200 Endovascular catheters

import

Dates and Status

Oct 24, 2011

Oct 24, 2021

Aug 15, 2023

Cancellation Information

Logged out

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