Taiwan FDA registration 7b61562b1b6be00524fd7380b4b65fbc
X-ray tube sleeve assembly for diagnostic "Shemokevi" (unsterilized)
TW: “舍摩凱維”診斷用X光球管套組件(未滅菌)
Registration details
- Analysis ID
- 7b61562b1b6be00524fd7380b4b65fbc
- Customs Code
- DHAS4400814502
Company information
- Manufacturer
- THERMO KEVEX
- Manufacturer Country
- United States
- Authorized Representative
- TRANSTEX CORPORATION
Product details
- Intended Use
- 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)".
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1760 診斷用X光球管套組件
- 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
- Sep 23, 2009
- Expiry Date
- Sep 23, 2014
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for X-ray tube sleeve assembly for diagnostic "Shemokevi" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7b61562b1b6be00524fd7380b4b65fbc and manufactured by THERMO KEVEX. The authorized representative in Taiwan is TRANSTEX CORPORATION.
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