Taiwan FDA registration 6dcab45377fc60f41a32f6bdbd459bdd

"Asia-Pacific Medical Federation" scalpel (sterilized/non-sterilized)

TW: "亞太醫聯" 手術刀 (滅菌/未滅菌)

Taiwan·Risk Class 1·KEHR SURGICAL PRIVATE LIMITED·Registered Mar 15, 2024 – Mar 15, 2029Active

Registration details

Analysis ID: 6dcab45377fc60f41a32f6bdbd459bdd
Customs Code: DHA09402342009

Company information

Manufacturer: KEHR SURGICAL PRIVATE LIMITED
Manufacturer Country: India
Authorized Representative: ASIA HEALTHCARE INC., TAIWAN BRANCH (BVI)

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: QMS/QSD;; 輸入

Dates and status

Registration Date: Mar 15, 2024
Expiry Date: Mar 15, 2029

About this record

Access comprehensive regulatory information for "Asia-Pacific Medical Federation" scalpel (sterilized/non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6dcab45377fc60f41a32f6bdbd459bdd and manufactured by KEHR SURGICAL PRIVATE LIMITED. The authorized representative in Taiwan is ASIA HEALTHCARE INC., TAIWAN BRANCH (BVI).

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.