Taiwan FDA registration c1efda5b97c85cd75f13473b1ce80d0b

Herda postoperative wound patch (sterilized)

TW: 赫爾達術後傷口貼 (滅菌)

Taiwan·Risk Class 1·TAICEND TECHNOLOGY CO., LTD.·Registered Jan 04, 2023 – Jan 04, 2028Active

Registration details

Analysis ID: c1efda5b97c85cd75f13473b1ce80d0b

Company information

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

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: Jan 04, 2023
Expiry Date: Jan 04, 2028

About this record

Access comprehensive regulatory information for Herda postoperative wound patch (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c1efda5b97c85cd75f13473b1ce80d0b and manufactured by TAICEND TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is TAICEND TECHNOLOGY CO., LTD..

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