Pure Global

"Philips" X-ray system - Taiwan Registration 932d21eee0708b53a8cecef0a260ea7b

Access comprehensive regulatory information for "Philips" X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 932d21eee0708b53a8cecef0a260ea7b and manufactured by Philips India limited;; Philips Medical Systems Nederland B.V.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Philips Medical Systems Nederland B.V., PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., and 5 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
5 Competitors
5 Recent Registrations
932d21eee0708b53a8cecef0a260ea7b
Registration Details
Taiwan FDA Registration: 932d21eee0708b53a8cecef0a260ea7b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Philips" X-ray system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ Xๅ…‰็ณป็ตฑ
Risk Class 2

Registration Details

932d21eee0708b53a8cecef0a260ea7b

DHAS5603723900

Company Information

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.1650 ้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

The consent of the Nuclear Safety Commission must be obtained for each import of this medical device.;; input

Dates and Status

Jun 23, 2024

Jun 23, 2029