Taiwan FDA registration c8e1da8f77f7aa5dc9451b0e1ab1da3b
"Crown Berry" gloves for patient examination (unsterilized)
TW: “克朗貝里”病患檢查用手套 (未滅菌)
Registration details
- Analysis ID
- c8e1da8f77f7aa5dc9451b0e1ab1da3b
- Customs Code
- DHA04400852007
Company information
- Manufacturer
- CRANBERRY (M) SDN. BHD.
- Manufacturer Country
- Malaysia
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Feb 06, 2010
- Expiry Date
- Feb 06, 2015
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Crown Berry" gloves for patient examination (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c8e1da8f77f7aa5dc9451b0e1ab1da3b and manufactured by CRANBERRY (M) SDN. BHD.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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