Taiwan FDA registration 2d4099e9dbdad45af1ef9f0f0df84082

Kjeldahl surgical blade (sterilized)

TW: “凱氏”手術用刀片(滅菌)

Taiwan·Risk Class 1·KAI INDUSTRIES CO., LTD.·Registered Aug 28, 2012 – Aug 28, 2027Active

Registration details

Analysis ID: 2d4099e9dbdad45af1ef9f0f0df84082
Customs Code: DHA04401212108

Company information

Manufacturer: KAI INDUSTRIES CO., LTD.
Manufacturer Country: Japan
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): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Aug 28, 2012
Expiry Date: Aug 28, 2027

About this record

Access comprehensive regulatory information for Kjeldahl surgical blade (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d4099e9dbdad45af1ef9f0f0df84082 and manufactured by KAI INDUSTRIES CO., LTD.. The authorized representative in Taiwan is HORIZON INSTRUMENTS CO. ,LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.