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"Philips" X-ray system - Taiwan Registration 3ed80a239cb4b5aae3baa525326056e2

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 3ed80a239cb4b5aae3baa525326056e2 and manufactured by PHILIPS AND NEUSOFT MEDICAL SYSTEMS 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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3ed80a239cb4b5aae3baa525326056e2
Registration Details
Taiwan FDA Registration: 3ed80a239cb4b5aae3baa525326056e2
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Device Details

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

Registration Details

3ed80a239cb4b5aae3baa525326056e2

DHAS4200014501

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

Chinese goods;; 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 03, 2006

Nov 03, 2011

Jan 17, 2013

Cancellation Information

Logged out

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