Taiwan FDA registration e6f513bfe234ba4038bde4a4a545b630

"Hongxiang" dermabrasive machine (unsterilized)

TW: “鴻祥” 磨皮機(未滅菌)

Taiwan·Risk Class 1·HONG SHIANG TECHNOLOGY CO., LTD.·Registered Nov 14, 2013 – Nov 14, 2028Active

Registration details

Analysis ID: e6f513bfe234ba4038bde4a4a545b630

Company information

Manufacturer: HONG SHIANG TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HONG SHIANG TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4820 Surgical Appliances and Accessories or Accessories
Import Information: Domestic

Dates and status

Registration Date: Nov 14, 2013
Expiry Date: Nov 14, 2028

About this record

Access comprehensive regulatory information for "Hongxiang" dermabrasive machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e6f513bfe234ba4038bde4a4a545b630 and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG TECHNOLOGY CO., LTD..

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