Taiwan FDA registration 33b6086f92a4463fa90af0bdc9a0c54c

High Clean Patient Examination Glove(Non-Sterile)

TW: 宏崟病患檢查用手套(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Professional Latex Sdn. Bhd.·Registered Oct 11, 2018 – Oct 11, 2023Expired
Registration details
Analysis ID
33b6086f92a4463fa90af0bdc9a0c54c
License Form
Ministry of Health Medical Device Import No. 019695
Customs Code
DHA09401969507
Company information
Manufacturer Country
Malaysia
Authorized Representative
HIGH CLEAN ENTERPRISE CO., LTD.
Product details
Intended Use
Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Gloves for Patient Examination (J.6250)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J6250 Gloves for patient examination
Import Information
Imported from abroad; GMP
Dates and status
Registration Date
Oct 11, 2018
Expiry Date
Oct 11, 2023
About this record

Access comprehensive regulatory information for High Clean 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 33b6086f92a4463fa90af0bdc9a0c54c and manufactured by Professional Latex Sdn. Bhd.. The authorized representative in Taiwan is HIGH CLEAN ENTERPRISE 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.

Free DatabasePowered by Pure Global AI89,000+ Devices