Taiwan FDA registration 973d618dfaca44b30364efdb898726ac

"Interwa" Jereh Non-powered Neurosurgical Instruments (Unsterilized)

TW: "英特華" 傑瑞非動力式神經外科用器械 (未滅菌)

Taiwan·Risk Class 1·INTEGRA YORK PA, INC.·Registered Jul 04, 2011 – Jul 04, 2021Cancelled

Registration details

Analysis ID: 973d618dfaca44b30364efdb898726ac
Customs Code: DHA04401053206

Company information

Manufacturer: INTEGRA YORK PA, INC.
Manufacturer Country: United States
Authorized Representative: Huizhong Co., Ltd

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4535 非動力式神經外科用器械
Import Information: import

Dates and status

Registration Date: Jul 04, 2011
Expiry Date: Jul 04, 2021
Cancellation Date: Oct 06, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Interwa" Jereh Non-powered Neurosurgical 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 973d618dfaca44b30364efdb898726ac and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is Huizhong Co., Ltd.

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