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"Philips" X-ray system - Taiwan Registration 23df7e5a27add47fbb9186e40c59fd0f

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 23df7e5a27add47fbb9186e40c59fd0f 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 India limited;; 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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23df7e5a27add47fbb9186e40c59fd0f
Registration Details
Taiwan FDA Registration: 23df7e5a27add47fbb9186e40c59fd0f
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Device Details

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

Registration Details

23df7e5a27add47fbb9186e40c59fd0f

DHAS0602416302

Company Information

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

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

Dates and Status

Nov 13, 2012

Nov 13, 2017

Dec 13, 2019

Cancellation Information

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