Pure Global

"Philips" positron/magnetic imaging system - Taiwan Registration 3d1cf0f521df186df4dc50a0b5643315

Access comprehensive regulatory information for "Philips" positron/magnetic imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d1cf0f521df186df4dc50a0b5643315 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. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
3d1cf0f521df186df4dc50a0b5643315
Registration Details
Taiwan FDA Registration: 3d1cf0f521df186df4dc50a0b5643315
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Philips" positron/magnetic imaging system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๆญฃๅญ/็ฃๆŒฏๅฝฑๅƒ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

3d1cf0f521df186df4dc50a0b5643315

DHA00602440607

Company Information

Product Details

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

P Radiology Science

P.1200 Radiology CT system

The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input

Dates and Status

Jan 31, 2013

Jan 31, 2018

Dec 13, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ