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“Stryker” LED Light Source - Taiwan Registration 2a9fc7ee5e5e9a309e658a48817f5c4e

Access comprehensive regulatory information for “Stryker” LED Light Source in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a9fc7ee5e5e9a309e658a48817f5c4e 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. 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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2a9fc7ee5e5e9a309e658a48817f5c4e
Registration Details
Taiwan FDA Registration: 2a9fc7ee5e5e9a309e658a48817f5c4e
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Device Details

“Stryker” LED Light Source
TW: “史賽克”醫用光源機
Risk Class 2
MD

Registration Details

2a9fc7ee5e5e9a309e658a48817f5c4e

Ministry of Health Medical Device Import No. 029724

DHA05602972400

Company Information

United States

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

May 17, 2017

May 17, 2027