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"Philips" X-ray system - Taiwan Registration 2afa9801f1e5439223a869c04b5fec0e

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 2afa9801f1e5439223a869c04b5fec0e and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH. 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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2afa9801f1e5439223a869c04b5fec0e
Registration Details
Taiwan FDA Registration: 2afa9801f1e5439223a869c04b5fec0e
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Device Details

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

Registration Details

2afa9801f1e5439223a869c04b5fec0e

DHAS0601285900

Company Information

Product Details

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

P Radiology Science

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

Oct 27, 2005

Oct 27, 2015

Apr 25, 2018

Cancellation Information

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