Taiwan FDA registration 5f6e39bf66ff8bc19a035d50554c1e1e

"H&H" wound gel (sterilized)

TW: 〝H&H〞傷口凝膠 (滅菌)

Taiwan·Risk Class 1·TRONJEN MEDICAL TECHNOLOGY INC.·Registered Dec 26, 2022 – Dec 26, 2027Active

Registration details

Analysis ID: 5f6e39bf66ff8bc19a035d50554c1e1e

Company information

Manufacturer: TRONJEN MEDICAL TECHNOLOGY INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TRONJEN MEDICAL TECHNOLOGY INC.

Product details

Intended Use: Limited to the first level recognition range of the classification and grading management measures for medical equipment "hydrophilic trauma covering materials (I.4018)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4018 親水性創傷覆蓋材
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Dec 26, 2022
Expiry Date: Dec 26, 2027

About this record

Access comprehensive regulatory information for "H&H" wound gel (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f6e39bf66ff8bc19a035d50554c1e1e and manufactured by TRONJEN MEDICAL TECHNOLOGY INC.. The authorized representative in Taiwan is TRONJEN MEDICAL TECHNOLOGY INC..

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