Taiwan FDA registration 23df7e5a27add47fbb9186e40c59fd0f

"Philips" X-ray system

TW: “飛利浦”X光系統
Taiwan flagTaiwan·Risk Class 2·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Nov 13, 2012 – Nov 13, 2017Cancelled
Registration details
Analysis ID
23df7e5a27add47fbb9186e40c59fd0f
Customs Code
DHAS0602416302
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.1680 固定式X光系統
Import Information
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Nov 13, 2012
Expiry Date
Nov 13, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
Companies making similar products

Top companies providing products similar to ""Philips" X-ray system"

Recent registrations

Recently registered similar products

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 23df7e5a27add47fbb9186e40c59fd0f 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.

Free DatabasePowered by Pure Global AI89,000+ Devices5 Competitors5 Recent Registrations