Taiwan FDA registration 0c7a8ab22b6938c9fae8471c81fe48b5
"KADEN" Wheeled Stretcher (Non-Sterile)
TW: "卡德"輪式擔床(未滅菌)
Taiwan·Risk Class 1·MD·KADEN INTERNATIONAL LTD.·Registered May 12, 2014 – May 12, 2019CancelledRegistration details
- Analysis ID
- 0c7a8ab22b6938c9fae8471c81fe48b5
- License Form
- Ministry of Health Medical Device Import No. 014122
- Customs Code
- DHA09401412200
Company information
- Manufacturer
- KADEN INTERNATIONAL LTD.
- Manufacturer Country
- Hong Kong
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6910 Wheeled stretcher
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 12, 2014
- Expiry Date
- May 12, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "KADEN" Wheeled Stretcher (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 0c7a8ab22b6938c9fae8471c81fe48b5 and manufactured by KADEN INTERNATIONAL LTD.. The authorized representative in Taiwan is PRO-READY 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