Taiwan FDA registration 1217ae8958e37249300a72b4e5bf7baa

"Medtronic" Hamilis heparin dose-response cassette

TW: "美敦力" 漢密思肝素劑量反應卡匣

Taiwan·Risk Class 2·MEDTRONIC PERFUSION SYSTEMS·Registered Jun 28, 2006 – Jun 28, 2011Cancelled

Registration details

Analysis ID: 1217ae8958e37249300a72b4e5bf7baa
Customs Code: DHA00601716902

Company information

Manufacturer: MEDTRONIC PERFUSION SYSTEMS
Manufacturer Country: United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: It is a device that measures the degree of response of whole blood to heparin.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.5680 Automated Heparin Analyzer
Import Information: import

Dates and status

Registration Date: Jun 28, 2006
Expiry Date: Jun 28, 2011
Cancellation Date: Nov 06, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Medtronic" Hamilis heparin dose-response cassette in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1217ae8958e37249300a72b4e5bf7baa and manufactured by MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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