31 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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BODYGUARDIAN SYSTEM BODYGUARDIAN CONTROL UNIT BODYGUARDIAN CONNECT
FDA 510(k)
FDA Class 2
·Cardiovascular
SURGISTAR, INC.
FDA UDI
SURGISTAR, INC.·00878799002242·
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780180241·Integra® Jarit® Sarot Needle Holder, 5-7/8", Ca...
NOVO Health Services, LLC
FDA UDI
NOVO HEALTH SERVICES, LLC·00812564031969·C-SECTION PACK
CHS
FDA UDI
Smith & Nephew, Inc.·03596010062697·Compression Hip Screw SUPER LAG SCREW 140MM
S 75-K
FDA UDI
BIOTRONIK SE & Co. KG·04035479145194·
ADVIA Centaur® VANC
FDA UDI
Siemens Healthcare Diagnostics Inc.·00630414443096·Vancomycin - CENTAUR - RGT - 250 tests
CORNEAL TREPHINE BLADE
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896012790·CORNEAL TREPHINE BLADE
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450585108·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197381055·Super-Cut Stevens Tenotomy Scissors
curved...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197040068·Super-Cut Stevens Tenotomy Scissors
10 cm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197040082·Super-Cut Stevens Tenotomy Scissors
curved...
BD VACUTAINER® SST¿ II ADVANCE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 30, 2025
BD VACUTAINER® SST¿ II ADVANCE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 30, 2025
BD VACUTAINER® SST¿ II ADVANCE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 30, 2025
BD VACUTAINER® SST¿ II ADVANCE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 30, 2025
BD VACUTAINER® SST¿ II ADVANCE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 30, 2025
BD VACUTAINER® SST¿ II ADVANCE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 30, 2025
SUREONE INSULIN SYRINGE, 31 GAUGE X 5/16
FDA 510(k)
FDA Class 2
·General Hospital
PARIE TENE PROGRIP MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery