Taiwan FDA registration c9930831d15aae27102615b5110d1a27

"Philips" X-ray system

TW: "飛利浦" X光系統
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Sep 20, 2005 – Sep 20, 2015Cancelled
Registration details
Analysis ID
c9930831d15aae27102615b5110d1a27
Customs Code
DHAS0601199602
Company information
Manufacturer Country
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.1600 X光血管攝影系統
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 20, 2005
Expiry Date
Sep 20, 2015
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
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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 c9930831d15aae27102615b5110d1a27 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, 5 companies making similar products including Philips Medical Systems Nederland B.V., Philips India limited;; 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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