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"Cordship" dry laser film (unsterilized) - Taiwan Registration e27733686738d3b089664dee8bdc80d1

Access comprehensive regulatory information for "Cordship" dry laser film (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e27733686738d3b089664dee8bdc80d1 and manufactured by CARESTREAM HEALTH, INC.. The authorized representative in Taiwan is FAITH BIOMED LTD..

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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e27733686738d3b089664dee8bdc80d1
Registration Details
Taiwan FDA Registration: e27733686738d3b089664dee8bdc80d1
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Device Details

"Cordship" dry laser film (unsterilized)
TW: "ๅบทไธ–" ไนพๅผ้›ทๅฐ„่ปŸ็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e27733686738d3b089664dee8bdc80d1

DHA04400022402

Company Information

United States

Product Details

Images can be recorded during diagnostic radiology.

P Radiology Science

P.1840 Radiographic film

import

Dates and Status

Jul 06, 2005

Jul 06, 2020

Jun 07, 2022

Cancellation Information

Logged out

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