Taiwan FDA registration d7ec5f8b5d7cc9f1e144da81f23e67cd

"Sebrondo" manual instruments for general surgery (unsterilized)

TW: “塞布朗恩朵”一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·SYBRONENDO·Registered Jul 26, 2012 – Jul 26, 2017Cancelled

Registration details

Analysis ID: d7ec5f8b5d7cc9f1e144da81f23e67cd
Customs Code: DHA04401198509

Company information

Manufacturer: SYBRONENDO
Manufacturer Country: United States
Authorized Representative: P & H BIOTECH CORP.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Jul 26, 2012
Expiry Date: Jul 26, 2017
Cancellation Date: Nov 26, 2019

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Sebrondo" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d7ec5f8b5d7cc9f1e144da81f23e67cd and manufactured by SYBRONENDO. The authorized representative in Taiwan is P & H BIOTECH CORP..

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