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"Philips" X-ray system - Taiwan Registration ba3605d404c478cf7d13b7b54a810300

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 ba3605d404c478cf7d13b7b54a810300 and manufactured by 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.

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ba3605d404c478cf7d13b7b54a810300
Registration Details
Taiwan FDA Registration: ba3605d404c478cf7d13b7b54a810300
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Device Details

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

Registration Details

ba3605d404c478cf7d13b7b54a810300

DHAS5603405205

Company Information

Product Details

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

P Radiology Science

P.1650 ้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Oct 13, 2020

Oct 13, 2025