Taiwan FDA registration dde15bc350281cf5d3da835d62788797

"Keesso" manual orthopedic surgical instruments (unsterilized)

TW: “基索”手動式骨科手術器械(未滅菌)

Taiwan·Risk Class 1·GSOURCE, LLC.·Registered May 15, 2012 – May 15, 2017Cancelled

Registration details

Analysis ID: dde15bc350281cf5d3da835d62788797
Customs Code: DHA04401170302

Company information

Manufacturer: GSOURCE, LLC.
Manufacturer Country: United States
Authorized Representative: Huixing Co., Ltd

Product details

Intended Use: Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.4540 手動式骨科手術器械
Import Information: import

Dates and status

Registration Date: May 15, 2012
Expiry Date: May 15, 2017
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Keesso" manual orthopedic surgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dde15bc350281cf5d3da835d62788797 and manufactured by GSOURCE, LLC.. The authorized representative in Taiwan is Huixing Co., Ltd.

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