Taiwan FDA registration 56ca075bac0dcf5ecd7b05defb67e879

"Sifotec" Lancet(Sterile)

TW: "和豐" 採血針(滅菌)

Taiwan·Risk Class 1·MD·SteriLance Medical (Suzhou) Inc.·Registered Nov 30, 2022 – Nov 30, 2027Active

Registration details

Analysis ID: 56ca075bac0dcf5ecd7b05defb67e879
License Form: Ministry of Health Medical Device Land Transport No. 004705
Customs Code: DHA09600470508

Company information

Manufacturer: SteriLance Medical (Suzhou) Inc.
Manufacturer Country: China
Authorized Representative: HORIZON INSTRUMENTS CO. ,LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Imported from abroad; GMP

Dates and status

Registration Date: Nov 30, 2022
Expiry Date: Nov 30, 2027

About this record

Access comprehensive regulatory information for "Sifotec" Lancet(Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 56ca075bac0dcf5ecd7b05defb67e879 and manufactured by SteriLance Medical (Suzhou) Inc.. The authorized representative in Taiwan is HORIZON INSTRUMENTS CO. ,LTD..

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