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"Philips" X-ray system - Taiwan Registration c9930831d15aae27102615b5110d1a27

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 c9930831d15aae27102615b5110d1a27 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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Registration Details
Taiwan FDA Registration: c9930831d15aae27102615b5110d1a27
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Device Details

"Philips" X-ray system
TW: "้ฃ›ๅˆฉๆตฆ" Xๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

c9930831d15aae27102615b5110d1a27

DHAS0601199602

Company Information

Product Details

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

P Radiology Science

P.1600 Xๅ…‰่ก€็ฎกๆ”ๅฝฑ็ณป็ตฑ

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

Sep 20, 2005

Sep 20, 2015

Apr 25, 2018

Cancellation Information

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