Taiwan FDA registration c7b46afb8564c1cec72237deaccc2a80

"Skyland" manual instruments for general surgery (unsterilized)

TW: "斯凱蘭"一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·SCANLAN INTERNATIONAL·Registered Jun 07, 2011 – Jun 07, 2016Cancelled

Registration details

Analysis ID: c7b46afb8564c1cec72237deaccc2a80
Customs Code: DHA04401045004

Company information

Manufacturer: SCANLAN INTERNATIONAL
Manufacturer Country: United States
Authorized Representative: PRO-READY ENTERPRISE CO., LTD.

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: Jun 07, 2011
Expiry Date: Jun 07, 2016
Cancellation Date: Aug 21, 2018

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Skyland" 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 c7b46afb8564c1cec72237deaccc2a80 and manufactured by SCANLAN INTERNATIONAL. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..

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