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"Thunderbolt" patient positioning beam indicator (not sterilized) - Taiwan Registration dfb8ed160c4d92ee0975c1edd2810581

Access comprehensive regulatory information for "Thunderbolt" patient positioning beam indicator (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dfb8ed160c4d92ee0975c1edd2810581 and manufactured by LAPLASER APPLIKATIONEN GMBH. The authorized representative in Taiwan is Exuberant International Enterprises Limited.

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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dfb8ed160c4d92ee0975c1edd2810581
Registration Details
Taiwan FDA Registration: dfb8ed160c4d92ee0975c1edd2810581
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Device Details

"Thunderbolt" patient positioning beam indicator (not sterilized)
TW: โ€œ้›ทๆณข้›ทๅฐ„โ€็—…ๆ‚ฃๅฎšไฝๅ…‰ๆŸๆŒ‡็คบๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dfb8ed160c4d92ee0975c1edd2810581

DHA04400510608

Company Information

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Equipment "Patient Positioning Beam Indicator (P.5780)".

P Radiology Science

P.5780 Patient Positioning Beam Indicator

import

Dates and Status

Aug 31, 2006

Aug 31, 2011

Nov 23, 2012

Cancellation Information

Logged out

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