Taiwan FDA registration 075f19ced5f70f45933dda867c7a64fe
"Henry" Patient Examination Gloves (Sterile/Unsterile)
TW: "軒瑞" 病患檢查用手套 (滅菌/未滅菌)
Taiwan·Risk Class 1·MULTISAFE SDN. BHD.·Registered Feb 13, 2015 – Feb 13, 2020CancelledRegistration details
- Analysis ID
- 075f19ced5f70f45933dda867c7a64fe
- Customs Code
- DHA09401492703
Company information
- Manufacturer
- MULTISAFE SDN. BHD.
- Manufacturer Country
- Malaysia
- Authorized Representative
- Xuanrui Technology Industrial 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)
- J.6250 病患檢查用手套
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Feb 13, 2015
- Expiry Date
- Feb 13, 2020
- Cancellation Date
- Feb 24, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Henry" Patient Examination Gloves (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 075f19ced5f70f45933dda867c7a64fe and manufactured by MULTISAFE SDN. BHD.. The authorized representative in Taiwan is Xuanrui Technology Industrial 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