Taiwan FDA registration 0bd25f036a791ab23085f25639579b55

"Kaiwei" introduction sleeve and its accessories (unsterilized)

TW: “愷威”導入套管及其附件(未滅菌)

Taiwan·Risk Class 1·KAI WEI (SHENZHEN) CO. LTD.·Registered May 25, 2006 – May 25, 2026Expired

Registration details

Analysis ID: 0bd25f036a791ab23085f25639579b55
Customs Code: DHA04600025302

Company information

Manufacturer: KAI WEI (SHENZHEN) CO. LTD.
Manufacturer Country: China
Authorized Representative: UNIMAX MEDICAL SYSTEMS INC.

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;; Chinese goods

Dates and status

Registration Date: May 25, 2006
Expiry Date: May 25, 2026

About this record

Access comprehensive regulatory information for "Kaiwei" introduction sleeve and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0bd25f036a791ab23085f25639579b55 and manufactured by KAI WEI (SHENZHEN) CO. LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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