100 results · 21ms · Sources: EU EUDAMED, 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