Taiwan FDA registration 135387841b63ccf5c87d9abaa7f43f1c

"Philips" Medical Image Transmission Device (Unsterilized)

TW: “飛利浦” 醫學影像傳輸裝置 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Registered Sep 17, 2012 – Sep 17, 2017Cancelled
Registration details
Analysis ID
135387841b63ccf5c87d9abaa7f43f1c
Customs Code
DHA04401217505
Company information
Manufacturer Country
Netherlands
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Limited to the first-level recognition range of medical image transmission devices (P.2020) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.2020 Medical imaging communication devices
Import Information
import
Dates and status
Registration Date
Sep 17, 2012
Expiry Date
Sep 17, 2017
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Philips" Medical Image Transmission Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 135387841b63ccf5c87d9abaa7f43f1c 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. 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+ Devices