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"Stryker" medical light source machine - Taiwan Registration 5ae6aa354108f05759cbd98526974013

Access comprehensive regulatory information for "Stryker" medical light source machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ae6aa354108f05759cbd98526974013 and manufactured by STRYKER ENDOSCOPY. 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 STRYKER ENDOSCOPY, and 2 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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5ae6aa354108f05759cbd98526974013
Registration Details
Taiwan FDA Registration: 5ae6aa354108f05759cbd98526974013
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Device Details

"Stryker" medical light source machine
TW: โ€œๅฒ่ณฝๅ…‹โ€้†ซ็”จๅ…‰ๆบๆฉŸ
Risk Class 2

Registration Details

5ae6aa354108f05759cbd98526974013

DHA00602052903

Company Information

United States

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Jan 18, 2010

Jan 18, 2025

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