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"Philips" cardiovascular X-ray system - Taiwan Registration d9c65f7c8f0bddfdd4283e49803d1e88

Access comprehensive regulatory information for "Philips" cardiovascular 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 d9c65f7c8f0bddfdd4283e49803d1e88 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, 2 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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d9c65f7c8f0bddfdd4283e49803d1e88
Registration Details
Taiwan FDA Registration: d9c65f7c8f0bddfdd4283e49803d1e88
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Device Details

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

Registration Details

d9c65f7c8f0bddfdd4283e49803d1e88

DHAS5602522601

Company Information

Product Details

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

P Radiology Science

P.1600 X-ray Vascular Photography System;; P.1650 Fluoroscopic X-ray Sensory Tube

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

Dates and Status

Aug 13, 2013

Aug 13, 2023

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