100 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MONOFILAMENT BIOSYN SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Troposphere
FDA UDI
HENRY SCHEIN, INC.·H65810000371·Troposphere Powder Fine Cut
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950023769·NEEDLEHOLDER MATHIEU MACHATT 5-1/2" 14CM
Bio2 Technologies
FDA UDI
BIO2 TECHNOLOGIES, INC.·B01010000371·VITRIUM E
18 x 7
e-vive TENS Electrode Set
FDA UDI
Motive Health, Inc.·00854816006943·e-vive TENS Electrode Set
AspireAssist First Year Kit, Magenta-US
FDA UDI
ASPIRE BARIATRICS, INC.·10857808005587·AspireAssist First Year Kit, Magenta-US
AP223-01 MICROBORE WITH NON-VENTED SPIKE, BACK CHECK VALVE, 0.2μ FILTER AND
FDA UDI
EITAN MEDICAL LTD·17290109150373·
QB1 NMES System
FDA UDI
Motive Health, Inc.·00854816006127·QB1 NMES System; X-LARGE, SHORT, RIGHT
PARSET SECONDARY ADMINISTRATION SET, LUERLOCK, MODEL A14001E, PARSET SECONDARY SECONDARY ADMINISTRATION SET, MODEL A1400
FDA 510(k)
FDA Class 2
·General Hospital
IMMULITE CARBAMAZEPINE, IMMULITE 2000 CARBAMAZEPINE, CATALOG # LKCB1, LKCB5 & L2KCB2, L2KCB6
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Panama™
FDA UDI
FLOSPINE LLC·B1830820000370·2-Level, 37mm Cervical Plate
AspireAssist First Year Kit, Magenta-LANG B
FDA UDI
ASPIRE BARIATRICS, INC.·10857808005396·AspireAssist First Year Kit, Magenta-LANG B
AspireAssist First Year Kit, Magenta-LANG C
FDA UDI
ASPIRE BARIATRICS, INC.·10857808005402·AspireAssist First Year Kit, Magenta-LANG C
AspireAssist First Year Kit, Magenta-LANG A
FDA UDI
ASPIRE BARIATRICS, INC.·10857808005389·AspireAssist First Year Kit, Magenta-LANG A
6000037-1999-00024
FDA Adverse Event
Injury
·December 29, 1999
6000037-1999-00026
FDA Adverse Event
Injury
·December 29, 1999
6000037-1999-00023
FDA Adverse Event
Injury
·December 29, 1999
SWEET TIP BIPOLAR LEAD
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS·Product code DXY·March 6, 1997
STEM: AMISTEM-P COLLARED LAT SIZE2
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·December 11, 2020
Heart-Valve, Mechanical
FDA Pre-Market Approval
FDA Class 3
·ON-X (R) PROSTHETIC HEART VALVE, MODEL ONXA