Taiwan FDA registration 43cb4d995c297860b254f319db61f951

"Antimony single" manual instruments for general surgery (unsterilized)

TW: “銻單”一般手術用手動式器械（未滅菌）

Taiwan·Risk Class 1·TEDAN SURGICAL INNOVATIONS·Registered Apr 02, 2013 – Apr 02, 2018Cancelled

Registration details

Analysis ID: 43cb4d995c297860b254f319db61f951
Customs Code: DHA04401286708

Company information

Manufacturer: TEDAN SURGICAL INNOVATIONS
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: Apr 02, 2013
Expiry Date: Apr 02, 2018
Cancellation Date: Dec 20, 2019

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Antimony single" 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 43cb4d995c297860b254f319db61f951 and manufactured by TEDAN SURGICAL INNOVATIONS. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..

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