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"Boston Tech" Combiguide guide tube - Taiwan Registration 000c27f913a3b0131258fbf4d2a4e8fe

Access comprehensive regulatory information for "Boston Tech" Combiguide guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 000c27f913a3b0131258fbf4d2a4e8fe and manufactured by PENDRACARE INTERNATIONAL B.V.. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.

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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000c27f913a3b0131258fbf4d2a4e8fe
Registration Details
Taiwan FDA Registration: 000c27f913a3b0131258fbf4d2a4e8fe
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Device Details

"Boston Tech" Combiguide guide tube
TW: โ€œๆณขๅฃซ้ “็ง‘ๆŠ€โ€ๅบทๅฟ…ๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2

Registration Details

000c27f913a3b0131258fbf4d2a4e8fe

DHA00602451104

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Mar 20, 2013

Mar 20, 2028