Medical Device
 State Department Issuing Safety-protection Provisions for Radioactive Isotope and Radiation-emitting Devices (2005-10-31 16:13:18)
 SFDA Seek Comments on the Classification of Products such as Scar Therapeutic Devices (2005-09-01 18:06:15)
 SFDA Seek Comments on “Supervision and Administration Provisions for the Circulation of Medical Devices” (2005-09-01 18:06:03)
 SFDA Solicits Public Comments on the Administrative Provisions for the Registration of in Vitro Diagnostic Reagents of Medical Devices (2004-07-29 09:53:47)
 SFDA Solicits Public Comments on Revised Administrative Provisions for Medical Device Manufacturer (2004-05-27 15:55:21)
 Revised Provisions for the Administration of Medical Devices Registration Ask for Comments (2004-04-13 08:53:12)
 SFDA Solicit Comments for the Newly Revised Administrative Provisions for the Manufacture of Medical Devices (2004-03-23 16:56:30)
 MOH Ceased Its Regulation on Single-Use Medical Devices (2003-12-01 10:45:24)
 SFDA Issued New Standards for Medical Device Industry (2003-10-16 09:01:48)
 Two sets of National Standards on Single-Use Devices for Comments (2003-09-28 11:22:51)
 SFDA Issued a Letter Requiring Comments Concerning Classification of Gels Used in Anti-allergen and Other Products (2003-09-27 11:18:28)
 SFDA: Determined to Strengthen the Administration of Medical Devices (2003-09-12 16:34:29)
 Supervision and Administration on Medical Protective Equipments Being Upgraded (2003-09-08 14:12:20)

 
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