Taiwan FDA registration f60acb6e59a771c6da92e9f596ed020b
"Shimadzu Radiation Cage"
TW: "島津放射線檯
Taiwan·Risk Class 1·SHIMADZU CORPORATION·Registered Mar 24, 2006 – Mar 24, 2016CancelledRegistration details
- Analysis ID
- f60acb6e59a771c6da92e9f596ed020b
- Customs Code
- DHA04400316909
Company information
- Manufacturer
- SHIMADZU CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- SAN KWANG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- 限醫療器材管理辦法「放射線檯(Radiographic table)[P.180]」第一等級鑑別範圍.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1980 Radiology
- Import Information
- import
Dates and status
- Registration Date
- Mar 24, 2006
- Expiry Date
- Mar 24, 2016
- Cancellation Date
- May 10, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Shimadzu Radiation Cage" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f60acb6e59a771c6da92e9f596ed020b and manufactured by SHIMADZU CORPORATION. The authorized representative in Taiwan is SAN KWANG INSTRUMENTS 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