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Philips radiation therapy simulation planning system - Taiwan Registration b3a3d03dcfd9b7072ae4e787e7c60816

Access comprehensive regulatory information for Philips radiation therapy simulation planning system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b3a3d03dcfd9b7072ae4e787e7c60816 and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHILIPS NUCLEAR MEDICINE, INC., and 1 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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b3a3d03dcfd9b7072ae4e787e7c60816
Registration Details
Taiwan FDA Registration: b3a3d03dcfd9b7072ae4e787e7c60816
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Device Details

Philips radiation therapy simulation planning system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๆ”พๅฐ„ๆฒป็™‚ๆจกๆ“ฌ่จˆ็•ซ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

b3a3d03dcfd9b7072ae4e787e7c60816

DHA00602208809

Company Information

Product Details

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

P Radiology Science

P.5840 Radiation therapy simulation system

import

Dates and Status

Mar 14, 2011

Mar 14, 2016

Apr 25, 2018

Cancellation Information

Logged out

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