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"Stryker" medical light source machine - Taiwan Registration 4b26e208a4fe1fba9f79836875197d52

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 4b26e208a4fe1fba9f79836875197d52 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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4b26e208a4fe1fba9f79836875197d52
Registration Details
Taiwan FDA Registration: 4b26e208a4fe1fba9f79836875197d52
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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

4b26e208a4fe1fba9f79836875197d52

DHA05603338608

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

Mar 13, 2020

Mar 13, 2030

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