Taiwan FDA registration 1f450c958c23a0c0903de4fda8246e7c

"Mestre" Patient Examination Gloves (Powder-free) (Non-sterile)

TW: "麥斯特" 病患檢查用手套 (無粉)(未滅菌)

Taiwan·Risk Class 1·MAXTER GLOVE MANUFACTURING SDN. BHD.·Registered Apr 24, 2024 – Apr 24, 2029Active

Registration details

Analysis ID: 1f450c958c23a0c0903de4fda8246e7c
Customs Code: DHA09402345604

Company information

Manufacturer: MAXTER GLOVE MANUFACTURING SDN. BHD.
Manufacturer Country: Malaysia
Authorized Representative: CONCERN LTD.

Product details

Intended Use: It is limited to the first level of identification of the "Gloves for Patient Examination (J.6250)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6250 病患檢查用手套
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Apr 24, 2024
Expiry Date: Apr 24, 2029

About this record

Access comprehensive regulatory information for "Mestre" Patient Examination Gloves (Powder-free) (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1f450c958c23a0c0903de4fda8246e7c and manufactured by MAXTER GLOVE MANUFACTURING SDN. BHD.. The authorized representative in Taiwan is CONCERN LTD..

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