Taiwan FDA registration caa3c6aeda6565427f3d813dcd6232b2

"Seihara" towing appendix (not sterilized)

TW: "聖原" 牽引用附件 (未滅菌)

Taiwan·Risk Class 1·Shengyuan Instrument Co., Ltd. Taoyuan Factory·Registered Feb 26, 2016 – Feb 26, 2021Cancelled

Registration details

Analysis ID: caa3c6aeda6565427f3d813dcd6232b2

Company information

Manufacturer: Shengyuan Instrument Co., Ltd. Taoyuan Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Shengyuan Instrument Co., Ltd. Taoyuan Factory

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Accessories for Traction (O.5925)".
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.5925 Reference Attachment
Import Information: Domestic

Dates and status

Registration Date: Feb 26, 2016
Expiry Date: Feb 26, 2021
Cancellation Date: Aug 15, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Seihara" towing appendix (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 caa3c6aeda6565427f3d813dcd6232b2 and manufactured by Shengyuan Instrument Co., Ltd. Taoyuan Factory. The authorized representative in Taiwan is Shengyuan Instrument Co., Ltd. Taoyuan Factory.

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