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"Boston Tech" Gade guide tube - Taiwan Registration 69730c2e8d324449425e3ea40e45a4fb

Access comprehensive regulatory information for "Boston Tech" Gade 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 69730c2e8d324449425e3ea40e45a4fb and manufactured by BOSTON SCIENTIFIC CORPORATION. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TARGET THERAPEUTICS INC. BESTON SCIENTIFIC CORPORATION, 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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69730c2e8d324449425e3ea40e45a4fb
Registration Details
Taiwan FDA Registration: 69730c2e8d324449425e3ea40e45a4fb
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Device Details

"Boston Tech" Gade guide tube
TW: โ€œๆณขๅฃซ้ “็ง‘ๆŠ€โ€่“‹ๅพทๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2

Registration Details

69730c2e8d324449425e3ea40e45a4fb

DHA00602125701

Company Information

United States

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

Jul 19, 2010

Jul 19, 2025

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