Pure Global

"Philips" diagnostic X-ray tube sleeve assembly (unsterilized)  - Taiwan Registration 5faf718f74301b0472fb200a2ea6fc1d

Access comprehensive regulatory information for "Philips" diagnostic X-ray tube sleeve assembly (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5faf718f74301b0472fb200a2ea6fc1d and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND) INC., DUNLEE DIV OF PH. MEDICAL SYSTEMS. 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 Database
Powered by Pure Global AI
89,000+ Devices
5faf718f74301b0472fb200a2ea6fc1d
Registration Details
Taiwan FDA Registration: 5faf718f74301b0472fb200a2ea6fc1d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Philips" diagnostic X-ray tube sleeve assembly (unsterilized) 
TW: “飛利浦”診斷用X光球管套組件 (未滅菌) 
Risk Class 1
Cancelled

Registration Details

5faf718f74301b0472fb200a2ea6fc1d

DHAS4400755401

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".

P Radiology Science

P.1760 診斷用X光球管套組件

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

Mar 16, 2009

Mar 16, 2014

Jan 09, 2017

Cancellation Information

Logged out

自行鍵入