Taiwan FDA registration 24f41ff815c645678357e465b51d8ff8

"Feile" scalpel (sterilized)

TW: “飛樂”手術刀 (滅菌)

Taiwan·Risk Class 1·FEATHER SAFETY RAZOR CO., LTD. MINO SITE·Registered Dec 20, 2019 – Dec 20, 2024Expired

Registration details

Analysis ID: 24f41ff815c645678357e465b51d8ff8
Customs Code: DHA09402112408

Company information

Manufacturer: FEATHER SAFETY RAZOR CO., LTD. MINO SITE
Manufacturer Country: Japan
Authorized Representative: RONG HSIN MEDICAL SUPPLY 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 20, 2019
Expiry Date: Dec 20, 2024

About this record

Access comprehensive regulatory information for "Feile" scalpel (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 24f41ff815c645678357e465b51d8ff8 and manufactured by FEATHER SAFETY RAZOR CO., LTD. MINO SITE. The authorized representative in Taiwan is RONG HSIN MEDICAL SUPPLY CO. LTD..

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