Taiwan FDA registration 3ed80a239cb4b5aae3baa525326056e2

"Philips" X-ray system

TW: "飛利浦"X光系統
Taiwan flagTaiwan·Risk Class 2·PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.·Registered Nov 03, 2006 – Nov 03, 2011Cancelled
Registration details
Analysis ID
3ed80a239cb4b5aae3baa525326056e2
Customs Code
DHAS4200014501
Company information
Manufacturer Country
China
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.1650 透視X光影像增感管
Import Information
Chinese goods;; 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 03, 2006
Expiry Date
Nov 03, 2011
Cancellation Date
Jan 17, 2013
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 3ed80a239cb4b5aae3baa525326056e2 and manufactured by PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD.. 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.

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