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"Kodak" dry laser printer - Taiwan Registration 0826c8f70f3d60c5ae63e66c9e632222

Access comprehensive regulatory information for "Kodak" dry laser printer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0826c8f70f3d60c5ae63e66c9e632222 and manufactured by CARESTREAM HEALTH, INC.. The authorized representative in Taiwan is Taiwan Kangshi Medical Equipment Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including RAYCO (SHANGHAI) MEDICAL PRODUCTS COMPANY LIMITED, CELESTICA (SUZHOU) TECHNOLOGY CO., LTD., and 3 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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0826c8f70f3d60c5ae63e66c9e632222
Registration Details
Taiwan FDA Registration: 0826c8f70f3d60c5ae63e66c9e632222
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Device Details

"Kodak" dry laser printer
TW: โ€œๆŸฏ้”โ€ไนพๅผ้›ทๅฐ„ๅฐ็‰‡ๆฉŸ
Risk Class 2
Cancelled

Registration Details

0826c8f70f3d60c5ae63e66c9e632222

DHA00601913903

Company Information

United States

Product Details

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

P Radiology Science

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import

Dates and Status

Jul 30, 2008

Jul 30, 2013

Jul 03, 2009

Cancellation Information

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