Taiwan FDA registration 78731755aa2c7b6b66a5b99f8f3982e8

"Philips" X-ray system

TW: “飛利浦” X光系統
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS DMC GMBH;; PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Sep 14, 2015 – Sep 14, 2025Expired
Registration details
Analysis ID
78731755aa2c7b6b66a5b99f8f3982e8
Customs Code
DHAS5602773200
Company information
Manufacturer Country
Germany;;Netherlands
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1680 固定式X光系統
Import Information
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
Registration Date
Sep 14, 2015
Expiry Date
Sep 14, 2025
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About this record

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 78731755aa2c7b6b66a5b99f8f3982e8 and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH;; 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 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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