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"Philips" mobile X-ray system - Taiwan Registration 31acbd172cc1cb1ba57fd1488d4709bd

Access comprehensive regulatory information for "Philips" mobile 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 31acbd172cc1cb1ba57fd1488d4709bd and manufactured by TECHNIX S. P. A.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including TECHNIX S. P. A., Philips Medical Systems Nederland B.V., and 2 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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31acbd172cc1cb1ba57fd1488d4709bd
Registration Details
Taiwan FDA Registration: 31acbd172cc1cb1ba57fd1488d4709bd
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Device Details

"Philips" mobile X-ray system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€็งปๅ‹•ๅผXๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

31acbd172cc1cb1ba57fd1488d4709bd

DHAS5602620202

Company Information

Italy

Product Details

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

P Radiology Science

P.1720 ็งปๅ‹•ๅผXๅ…‰็ณป็ตฑ

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

May 19, 2014

May 19, 2019

Jul 15, 2022

Cancellation Information

Logged out

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