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“Boston Scientific” Wallstent Super Stiff Guidewire - Taiwan Registration 67dca831a205715c60502cf750d82102

Access comprehensive regulatory information for “Boston Scientific” Wallstent Super Stiff Guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67dca831a205715c60502cf750d82102 and manufactured by LAKE REGION MEDICAL. 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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67dca831a205715c60502cf750d82102
Registration Details
Taiwan FDA Registration: 67dca831a205715c60502cf750d82102
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Device Details

“Boston Scientific” Wallstent Super Stiff Guidewire
TW: “波士頓科技”華斯登導引線
Risk Class 2
MD
Cancelled

Registration Details

67dca831a205715c60502cf750d82102

Ministry of Health Medical Device Import No. 025305

DHA05602530502

Company Information

United States

Product Details

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Jul 27, 2013

Jul 27, 2018

Jun 22, 2022

Cancellation Information

Logged out

許可證已逾有效期