"Wenli Asia Pacific" Delmar Inspection Gloves (Powder-free) (Unsterilized) - Taiwan Registration 55fc033e1d0277f296dc59b9496845b3
Access comprehensive regulatory information for "Wenli Asia Pacific" Delmar Inspection Gloves (Powder-free) (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55fc033e1d0277f296dc59b9496845b3 and manufactured by WRP ASIA PACIFIC SDN BHD. The authorized representative in Taiwan is SANSOME TRADING CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
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)".
J General hospital and personal use equipment
J.6250 ็ ๆฃๆชขๆฅ็จๆๅฅ
Input;; QMS/QSD
Dates and Status
Aug 26, 2010
Aug 26, 2025

