Taiwan FDA registration ed91248fd60ebeada2ecf137f685b718

"芮柏芙" manual surgical instrument (unsterilized)

TW: "芮柏芙" 手動式外科器械(未滅菌)

Taiwan·Risk Class 1·ZEPF MEDICAL INSTRUMENTS GMBH·Registered Dec 30, 2022 – Dec 30, 2027Active

Registration details

Analysis ID: ed91248fd60ebeada2ecf137f685b718
Customs Code: DHA09402299503

Company information

Manufacturer: ZEPF MEDICAL INSTRUMENTS GMBH
Manufacturer Country: Germany
Authorized Representative: HIGH TOP MEDICAL 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): I.4800 Hand Instruments for General Surgery
Import Information: Input;; QMS/QSD

Dates and status

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

About this record

Access comprehensive regulatory information for "芮柏芙" manual surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ed91248fd60ebeada2ecf137f685b718 and manufactured by ZEPF MEDICAL INSTRUMENTS GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL CO., LTD..

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