Taiwan FDA registration e97d0bb26dc1c683d5e6d5b993f34bd1
"Fengquan" plastic examination gloves (unsterilized)
TW: “豐全”塑膠檢診手套（未滅菌）
Taiwan·Risk Class 1·SHANDONG JIAZHAN PLASTIC PRODUCTS CO., LTD.·Registered Jun 21, 2010 – Jun 21, 2015CancelledRegistration details
- Analysis ID
- e97d0bb26dc1c683d5e6d5b993f34bd1
- Customs Code
- DHA04600095801
Company information
- Manufacturer
- SHANDONG JIAZHAN PLASTIC PRODUCTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- FOR CARE 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)
- J.6250 病患檢查用手套
- Import Information
- Input;; QMS/QSD;; Chinese goods
Dates and status
- Registration Date
- Jun 21, 2010
- Expiry Date
- Jun 21, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Fengquan" plastic examination gloves (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e97d0bb26dc1c683d5e6d5b993f34bd1 and manufactured by SHANDONG JIAZHAN PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is FOR CARE 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