Taiwan FDA registration e2f1f60acbbc35595c7004e28148b528

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

TW: "雅氏"一般手術用手動式器械(未滅菌)

Taiwan·Risk Class 1·MD·AESCULAP CHIFA SP. Z O.O.·Registered Jan 09, 2014 – Jan 09, 2024Expired

Registration details

Analysis ID: e2f1f60acbbc35595c7004e28148b528
License Form: Ministry of Health Medical Device Import No. 013767
Customs Code: DHA09401376702

Company information

Manufacturer: AESCULAP CHIFA SP. Z O.O.
Manufacturer Country: Poland
Authorized Representative: B. BRAUN TAIWAN 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: Jan 09, 2014
Expiry Date: Jan 09, 2024

About this record

Access comprehensive regulatory information for "Aesculap" 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 e2f1f60acbbc35595c7004e28148b528 and manufactured by AESCULAP CHIFA SP. Z O.O.. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

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