Taiwan FDA registration 1cd164714db0ea70378ff63be20ed06f

"Kaiwei" scraper (unsterilized)

TW: “愷威”刮器(未滅菌)

Taiwan·Risk Class 1·KAIWEI (SHENZHEN) CO., LTD.·Registered Apr 20, 2010 – Apr 20, 2025Expired

Registration details

Analysis ID: 1cd164714db0ea70378ff63be20ed06f
Customs Code: DHA04600090503

Company information

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

Product details

Intended Use: It is limited to the first-level identification scope of the "Laparoscope and its Accessories for Obstetrics and Gynecology (L.1720)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): l Obstetrics and Gynecology
Product Type (Level 2): L.1720 Gynecology and gynecologic laparoscopes and their appendages
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Apr 20, 2010
Expiry Date: Apr 20, 2025

About this record

Access comprehensive regulatory information for "Kaiwei" scraper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1cd164714db0ea70378ff63be20ed06f and manufactured by KAIWEI (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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