Taiwan FDA registration 52f50503a3257de02f184d8ba65c3ab3

"Magic Control" anticoagulant dosimetry

TW: "奇魔控" 抗凝劑量測定

Taiwan·Risk Class 2·Accriva Diagnostics Inc., dba ITC, dba Accumetrics·Registered May 11, 2006 – May 11, 2021Cancelled

Registration details

Analysis ID: 52f50503a3257de02f184d8ba65c3ab3
Customs Code: DHA00601658906

Company information

Manufacturer: Accriva Diagnostics Inc., dba ITC, dba Accumetrics
Manufacturer Country: United States
Authorized Representative: TRANSMEDIC CO., LTD.

Product details

Intended Use: Used to assess heparin dose response in vitro.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.7525 Heparin analysis
Import Information: import

Dates and status

Registration Date: May 11, 2006
Expiry Date: May 11, 2021
Cancellation Date: Sep 23, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Magic Control" anticoagulant dosimetry in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52f50503a3257de02f184d8ba65c3ab3 and manufactured by Accriva Diagnostics Inc., dba ITC, dba Accumetrics. The authorized representative in Taiwan is TRANSMEDIC CO., LTD..

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