"WRP" Patient Examination Glove (Non-Sterile) - Taiwan Registration 4b2695049410c037a1f95de75f4ed839
Access comprehensive regulatory information for "WRP" Patient Examination Glove (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 4b2695049410c037a1f95de75f4ed839 and manufactured by WRP ASIA PACIFIC SDN BHD. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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
Registration Details
4b2695049410c037a1f95de75f4ed839
Ministry of Health Medical Device Import No. 018734
DHA09401873402
Product Details
Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Gloves for Patient Examination (J.6250)".
J General hospital and personal use equipment
J6250 Gloves for patient examination
Imported from abroad; GMP
Dates and Status
Jan 17, 2018
Jan 17, 2028