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"Philips" X-ray system - Taiwan Registration cf0bcc3e934de2f7e835ce50e9dce04f

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 cf0bcc3e934de2f7e835ce50e9dce04f and manufactured by Philips Healthcare (Suzhou) Co., Ltd. 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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cf0bcc3e934de2f7e835ce50e9dce04f
Registration Details
Taiwan FDA Registration: cf0bcc3e934de2f7e835ce50e9dce04f
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Device Details

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

Registration Details

cf0bcc3e934de2f7e835ce50e9dce04f

DHAS9200085700

Company Information

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

Chinese goods;; Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Aug 01, 2017

Aug 01, 2022

Apr 12, 2024

Cancellation Information

Logged out

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