Taiwan FDA registration 31acbd172cc1cb1ba57fd1488d4709bd

"Philips" mobile X-ray system

TW: “飛利浦”移動式X光系統
Taiwan flagTaiwan·Risk Class 2·TECHNIX S. P. A.·Registered May 19, 2014 – May 19, 2019Cancelled
Registration details
Analysis ID
31acbd172cc1cb1ba57fd1488d4709bd
Customs Code
DHAS5602620202
Company information
Manufacturer
TECHNIX S. P. A.
Manufacturer Country
Italy
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.1720 移動式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
May 19, 2014
Expiry Date
May 19, 2019
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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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