Taiwan FDA registration 5909b16a0b36df072f081f4cb183c7a2

Postoperative wound dressings (unsterilized/sterilized)

TW: 〝H&H〞術後傷口敷料 (未滅菌/滅菌)

Taiwan·Risk Class 1·TRONJEN MEDICAL TECHNOLOGY INC.·Registered Aug 30, 2018 – Aug 30, 2028Active

Registration details

Analysis ID: 5909b16a0b36df072f081f4cb183c7a2

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: 國產;; QMS/QSD

Dates and status

Registration Date: Aug 30, 2018
Expiry Date: Aug 30, 2028

About this record

Access comprehensive regulatory information for Postoperative wound dressings (unsterilized/sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5909b16a0b36df072f081f4cb183c7a2 and manufactured by TRONJEN MEDICAL TECHNOLOGY INC.. The authorized representative in Taiwan is TRONJEN MEDICAL TECHNOLOGY INC..

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