Taiwan FDA registration 7545ecb4eb2ee61d64aa60e2fe1deedf

"Junkang" Medical Examination Gloves (Powder-Free/Non-Sterile)

TW: "雋康" 醫檢手套 (無粉/未滅菌)

Taiwan·Risk Class 1·INPRO TECHNOLOGY DEVICE FACTORY CO., LTD·Registered Feb 20, 2024 – Feb 20, 2029Active

Registration details

Analysis ID: 7545ecb4eb2ee61d64aa60e2fe1deedf
Customs Code: DHA09600488905

Company information

Manufacturer: INPRO TECHNOLOGY DEVICE FACTORY CO., LTD
Manufacturer Country: China
Authorized Representative: EVERJK ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Equipment "Gloves for Patient Examination (J.6250)".
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;; Chinese goods;; QMS/QSD

Dates and status

Registration Date: Feb 20, 2024
Expiry Date: Feb 20, 2029

About this record

Access comprehensive regulatory information for "Junkang" Medical 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 7545ecb4eb2ee61d64aa60e2fe1deedf and manufactured by INPRO TECHNOLOGY DEVICE FACTORY CO., LTD. The authorized representative in Taiwan is EVERJK ENTERPRISE CO., LTD..

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