Taiwan FDA registration 2257ebdbf87a4def23d16e42d8acf03b

"Kubota" blood vault eccentricity machine (not sterilized)

TW: "久保田"血庫離心機(未滅菌)

Taiwan·Risk Class 1·KUBOTA MFG. CORP. FUJIOKA PLANT·Registered Aug 28, 2008 – Aug 28, 2018Cancelled

Registration details

Analysis ID: 2257ebdbf87a4def23d16e42d8acf03b
Customs Code: DHA04400702403

Company information

Manufacturer: KUBOTA MFG. CORP. FUJIOKA PLANT
Manufacturer Country: Japan
Authorized Representative: DOUBLE EAGLE ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9275 Blood bank centrifuge for in vitro diagnostics
Import Information: import

Dates and status

Registration Date: Aug 28, 2008
Expiry Date: Aug 28, 2018
Cancellation Date: Jun 22, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Kubota" blood vault eccentricity machine (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 2257ebdbf87a4def23d16e42d8acf03b and manufactured by KUBOTA MFG. CORP. FUJIOKA PLANT. The authorized representative in Taiwan is DOUBLE EAGLE ENTERPRISE CO., LTD..

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