Taiwan FDA registration b632f639179c0b88543e30a696d9e0d1

"Artima" manual instruments for general surgery (unsterilized)

TW: “阿緹瑪”一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·ULTIMATE MEDICAL PRODUCTS LTD.·Registered Nov 27, 2007 – Nov 27, 2012Cancelled

Registration details

Analysis ID: b632f639179c0b88543e30a696d9e0d1
Customs Code: DHA04400632400

Company information

Manufacturer: ULTIMATE MEDICAL PRODUCTS LTD.
Manufacturer Country: United Arab Emirates
Authorized Representative: Liren Equipment Factory 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: Nov 27, 2007
Expiry Date: Nov 27, 2012
Cancellation Date: Apr 16, 2014

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Artima" 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 b632f639179c0b88543e30a696d9e0d1 and manufactured by ULTIMATE MEDICAL PRODUCTS LTD.. The authorized representative in Taiwan is Liren Equipment Factory Co., Ltd.

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