Taiwan FDA registration 9848383be05cc9442a85b56292934927

"Anker" patient positioning beam indicator (not sterilized)

TW: "安克" 病患定位光束指示器 (未滅菌)

Taiwan·Risk Class 1·Xinghe Biomedical Co., Ltd. Taichung Factory·Registered Mar 29, 2019 – Mar 29, 2024Expired

Registration details

Analysis ID: 9848383be05cc9442a85b56292934927

Company information

Manufacturer: Xinghe Biomedical Co., Ltd. Taichung Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: AMCAD BIOMED CORPORATION

Product details

Intended Use: Limited to the first level identification range of the "Patient Positioning Beam Indicator (P.5780)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.5780 Patient Positioning Beam Indicator
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Mar 29, 2019
Expiry Date: Mar 29, 2024

About this record

Access comprehensive regulatory information for "Anker" patient positioning beam indicator (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9848383be05cc9442a85b56292934927 and manufactured by Xinghe Biomedical Co., Ltd. Taichung Factory. The authorized representative in Taiwan is AMCAD BIOMED 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.