Taiwan FDA registration 557253f616ead6d4b50d3ad230434b45

"ATitan" Manual Surgical Instrument for General Use (Non-Sterile)

TW: "艾迪登" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·ATI(ATITAN INSTRUMENTS), ARNOLD TUBER INDUSTRIES LLC·Registered Aug 18, 2017 – Aug 18, 2022Expired

Registration details

Analysis ID: 557253f616ead6d4b50d3ad230434b45
License Form: Ministry of Health Medical Device Import No. 018211
Customs Code: DHA09401821106

Company information

Manufacturer: ATI(ATITAN INSTRUMENTS), ARNOLD TUBER INDUSTRIES LLC
Manufacturer Country: United States
Authorized Representative: HUNG KUO MEDICAL INSTRUMENT 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 and plastic surgical devices
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 18, 2017
Expiry Date: Aug 18, 2022

About this record

Access comprehensive regulatory information for "ATitan" Manual Surgical Instrument for General Use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 557253f616ead6d4b50d3ad230434b45 and manufactured by ATI(ATITAN INSTRUMENTS), ARNOLD TUBER INDUSTRIES LLC. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..

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