Taiwan FDA registration 33b6086f92a4463fa90af0bdc9a0c54c
High Clean Patient Examination Glove(Non-Sterile)
TW: 宏崟病患檢查用手套(未滅菌)
Registration details
- Analysis ID
- 33b6086f92a4463fa90af0bdc9a0c54c
- License Form
- Ministry of Health Medical Device Import No. 019695
- Customs Code
- DHA09401969507
Company information
- Manufacturer
- Professional Latex Sdn. Bhd.
- 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