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"Karst" Plastic Surgery Kit and its Accessories (Unsterilized) - Taiwan Registration cc0044e9c2c78ac95fb15dbbeb2cb81f

Access comprehensive regulatory information for "Karst" Plastic Surgery Kit 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 cc0044e9c2c78ac95fb15dbbeb2cb81f and manufactured by KARL STORZ SE & Co. KG;; Karl Storz SE & Co. KG. The authorized representative in Taiwan is KARL STORZ ENDOSCOPY TAIWAN 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.

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Registration Details
Taiwan FDA Registration: cc0044e9c2c78ac95fb15dbbeb2cb81f
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Device Details

"Karst" Plastic Surgery Kit and its Accessories (Unsterilized)
TW: โ€œๅก็ˆพๆ–ฏ็‰นโ€ๆ•ดๅฝขๅค–็ง‘ๆ‰‹่ก“็ต„ๅฅ—ๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

cc0044e9c2c78ac95fb15dbbeb2cb81f

DHA04400736707

Company Information

Product Details

It is limited to the scope of the first level of identification of the orthopedic surgery set and its accessories (I.3925) of the Classification and Grading Management Measures for Medical Devices.

I General, Plastic Surgery and Dermatology

I.3925 Orthopaedic surgical kit and its accessories

Input;; QMS/QSD

Dates and Status

Jan 06, 2009

Jan 06, 2029