Taiwan FDA registration fbbd1a4b27b8d830c446872a249853a5

"Acereys" plasma organ volumetric test system (unsterilized)

TW: “艾思瑞斯”血漿器官體積計測法試驗系統(未滅菌)

Taiwan·Risk Class 1·ARTHREX INC.·Registered Jul 16, 2010 – Jul 16, 2015Cancelled

Registration details

Analysis ID: fbbd1a4b27b8d830c446872a249853a5
Customs Code: DHA04400899301

Company information

Manufacturer: ARTHREX INC.
Manufacturer Country: United States
Authorized Representative: CHAWEI CO., LTD.

Product details

Intended Use: It is limited to the first level of identification of the plasma organ volume measurement test system (A.1530) of the Medical Device Management Measures.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1530 Plasma Organ Product Measurement Method
Import Information: import

Dates and status

Registration Date: Jul 16, 2010
Expiry Date: Jul 16, 2015
Cancellation Date: Jun 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Acereys" plasma organ volumetric test system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fbbd1a4b27b8d830c446872a249853a5 and manufactured by ARTHREX INC.. The authorized representative in Taiwan is CHAWEI 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.