Taiwan FDA registration d62d9f049b2746c6a93e2dd5512704b7

Autoclave generator for X-ray machine for diagnostic "gitt" (unsterilized)

TW: “吉特”診斷用X光機高壓產生器(未滅菌)

Taiwan·Risk Class 1·GTR LABS, INC.·Registered Jul 19, 2007 – Jul 19, 2017Cancelled

Registration details

Analysis ID: d62d9f049b2746c6a93e2dd5512704b7
Customs Code: DHAS4400601709

Company information

Manufacturer: GTR LABS, INC.
Manufacturer Country: United States
Authorized Representative: WITTECH CO., LTD.

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "X-ray Machine High Voltage Generator for Diagnosis (P.1700)".
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.1700 診斷用X光機高壓產生器
Import Information: Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); QMS/QSD;; input

Dates and status

Registration Date: Jul 19, 2007
Expiry Date: Jul 19, 2017
Cancellation Date: Nov 17, 2019

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for Autoclave generator for X-ray machine for diagnostic "gitt" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d62d9f049b2746c6a93e2dd5512704b7 and manufactured by GTR LABS, INC.. The authorized representative in Taiwan is WITTECH CO., LTD..

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.