Taiwan FDA registration f4240030c011124330d30555af1a9582

"Abbott" EDTA capillary blood collection tube (unsterilized)

TW: ”亞培” EDTA毛細血液採集管 (未滅菌)

Taiwan·Risk Class 1·Abbott Diagnostics Medical Co., Ltd.-Chiba Plant.·Registered Dec 02, 2010 – Dec 02, 2025Expired

Registration details

Analysis ID: f4240030c011124330d30555af1a9582
Customs Code: DHA04400960303

Company information

Manufacturer: Abbott Diagnostics Medical Co., Ltd.-Chiba Plant.
Manufacturer Country: Japan
Authorized Representative: Abbott Rapid Diagnostics Health Corp.

Product details

Intended Use: It is limited to the first level of identification scope of the "Capillary Blood Collection Tube (B.6150)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.6150 Capillary Blood Collection Tubes
Import Information: import

Dates and status

Registration Date: Dec 02, 2010
Expiry Date: Dec 02, 2025

About this record

Access comprehensive regulatory information for "Abbott" EDTA capillary blood collection tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4240030c011124330d30555af1a9582 and manufactured by Abbott Diagnostics Medical Co., Ltd.-Chiba Plant.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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