Taiwan FDA registration 62059bd5bbae07854cfd59d8610f2bf7

"Qinda" hydrophilic wound dressing (sterilized)

TW: “勤達”親水性創傷敷料 (滅菌)

Taiwan·Risk Class 1·BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.·Registered Jul 22, 2008 – Jul 22, 2023Expired

Registration details

Analysis ID: 62059bd5bbae07854cfd59d8610f2bf7
Customs Code: DHA04600053601

Company information

Manufacturer: BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
Manufacturer Country: China
Authorized Representative: TEAM POWER MEDICAL INSTRUMENT LTD.

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound 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;; Input;; Chinese goods

Dates and status

Registration Date: Jul 22, 2008
Expiry Date: Jul 22, 2023

About this record

Access comprehensive regulatory information for "Qinda" hydrophilic wound dressing (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 62059bd5bbae07854cfd59d8610f2bf7 and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..

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