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Philips radiation therapy simulation planning system - Taiwan Registration 375992d66e79a744d4449ecbfb96b7a2

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 375992d66e79a744d4449ecbfb96b7a2 and manufactured by PHILIPS NUCLEAR MEDICINE, 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 MEDICAL SYSTEMS(CLEVELAND),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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375992d66e79a744d4449ecbfb96b7a2
Registration Details
Taiwan FDA Registration: 375992d66e79a744d4449ecbfb96b7a2
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Device Details

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

Registration Details

375992d66e79a744d4449ecbfb96b7a2

DHA00601849000

Company Information

United States

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

Dec 11, 2007

Dec 11, 2012

Jul 25, 2014

Cancellation Information

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