Taiwan FDA registration 932d21eee0708b53a8cecef0a260ea7b

"Philips" X-ray system

TW: “飛利浦” X光系統
Taiwan flagTaiwan·Risk Class 2·Philips India limited;; Philips Medical Systems Nederland B.V.·Registered Jun 23, 2024 – Jun 23, 2029Active
Registration details
Analysis ID
932d21eee0708b53a8cecef0a260ea7b
Customs Code
DHAS5603723900
Company information
Manufacturer Country
Netherlands;;India
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1650 透視X光影像增感管
Import Information
The consent of the Nuclear Safety Commission must be obtained for each import of this medical device.;; input
Dates and status
Registration Date
Jun 23, 2024
Expiry Date
Jun 23, 2029
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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 932d21eee0708b53a8cecef0a260ea7b and manufactured by Philips India limited;; 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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