37 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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GLOBAL UNITE Platform Shoulder System
FDA 510(k)
FDA Class 2
·Orthopedic
OsteoMed
FDA UDI
OSTEOMED LLC·00845694020046·FPS 2.7mm x 10mm Standard Screw
Plateau-C Ti
FDA UDI
Life Spine, Inc.·00190837067274·Custom Small Anatomical Spacer, 7degree, 10mm
PMT CORPORATION
FDA UDI
PMT CORPORATION·00650551149972·INTERCONNECTION CABLE, 40 CONTACT (10X4) , INLI...
PMT CORPORATION
FDA UDI
PMT CORPORATION·00650551148050·10 CONTACT INTERCONNECTION CABLE, Y-SPLIT INLIN...
PMT CORPORATION
FDA UDI
PMT CORPORATION·00650551147831·INTERCONNECTION CABLE, 20 CONTACT, INLINE CONNE...
N/A
FDA UDI
PMT CORPORATION·00650551142928·INTERCONNECTION CABLE, 10 CONTACT (10X1), INLIN...
Vu a-POD™
FDA UDI
Seaspine Orthopedics Corporation·10889981038090·27x21mm Trial 10mm 12 deg. The Vu a-POD interve...
BD LUER-LOK¿ DISPOSABLE SYRINGE WITH BD LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·January 15, 2018
ZENOTEC ZR BRIDGE, ZENOSTAR ZR TRANSLUCENT, ZENOTEC COLOR ZR, ZENOSTAR COLOR ZR
FDA 510(k)
FDA Class 2
·Dental
DISPOSABLE POWDERED VINYL EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
OsteoMed
FDA UDI
OSTEOMED LLC·00845694073905·FPS 2.7 x 10mm Screw Sterile Qty 5
PMT CORPORATION
FDA UDI
PMT CORPORATION·00650551148067·10 CONTACT INTERCONNECTION CABLE, Y-SPLIT INLIN...
N/A
FDA UDI
PMT CORPORATION·00650551143024·INTERCONNECTION CABLE, 10 CONTACT (10X1), INLIN...
PMT CORPORATION
FDA UDI
PMT CORPORATION·00650551148500·INTERCONNECTION CABLE, 20 CONTACT, INLINE CONNE...
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE (SG)·Product code FRN·October 29, 2008
OMNIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·July 12, 2011
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 9, 2013
MAX PRI DCM TIB BRNG14X71/75MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 28, 2017
MAXIM POR ANA PRI FML 65 LT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·September 28, 2017