Taiwan FDA registration 2c5981be34632a3aa127932ba53c262d

"Etixi" hand jika hemostasis time measurement equipment (sterilization)

TW: 〝艾帝西〞手吉卡止血時間測定器材(滅菌)

Taiwan·Risk Class 1·Accriva Diagnostics Inc.·Registered Jul 18, 2012 – Jul 18, 2027Active

Registration details

Analysis ID: 2c5981be34632a3aa127932ba53c262d
Customs Code: DHA04401195704

Company information

Manufacturer: Accriva Diagnostics Inc.
Manufacturer Country: United States
Authorized Representative: BioChain Co., Ltd.

Product details

Intended Use: It is limited to the first level of identification scope of the "Bleeding Time Measurement Device (B.6100)" 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.6100 Bleeding Time Measuring Apparatus
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jul 18, 2012
Expiry Date: Jul 18, 2027

About this record

Access comprehensive regulatory information for "Etixi" hand jika hemostasis time measurement equipment (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2c5981be34632a3aa127932ba53c262d and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is BioChain Co., Ltd..

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