Pt. Mandiri Inti Buana is one of 6 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.
Pt. Mandiri Inti Buana - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Pt. Mandiri Inti Buana has 4 FDA 510(k) cleared medical devices. Based in Medan, ID.
Historical record: 4 cleared submissions from 2003 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pt. Mandiri Inti Buana Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pt. Mandiri Inti Buana
4 devices
Cleared
Oct 06, 2005
FLEXISKIN POLYMER COATED LATEX EXAMINATION GLOVES, POWDER FREE, NON-STERILE
General Hospital
76d
Cleared
Dec 16, 2004
FLEXISKIN POWDER FREE NITRILE EXAMINATION GLOVES, NON STERILE
General Hospital
120d
Cleared
Jun 30, 2003
FLEXISKIN POWDER FREE LATEX EXAMINATION GLOVES, NON STERILE
General Hospital
91d
Cleared
May 21, 2003
FLEXISKIN LATEX EXAMINATION GLOVES, POWDERED, NON STERILE
General Hospital
51d