Taiwan FDA registration a2bac9b2d1bb83c5dfaf7916de004d4d

"Jianxin" hydrogel wound dressing (unsterilized)

TW: “健鑫”水凝膠傷口敷料 (未滅菌)

Taiwan·Risk Class 1·JIANXIN BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Oct 16, 2013 – Oct 16, 2028Active

Registration details

Analysis ID: a2bac9b2d1bb83c5dfaf7916de004d4d

Company information

Manufacturer: JIANXIN BIOMEDICAL TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: JIANXIN BIOMEDICAL TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level of classification and grading management of medical equipment "Waterborne Wound and Burn Covering (I.4022)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4022 Water-based wounds and burn covers
Import Information: Domestic

Dates and status

Registration Date: Oct 16, 2013
Expiry Date: Oct 16, 2028

About this record

Access comprehensive regulatory information for "Jianxin" hydrogel wound dressing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a2bac9b2d1bb83c5dfaf7916de004d4d and manufactured by JIANXIN BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is JIANXIN BIOMEDICAL TECHNOLOGY CO., LTD..

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