34 results · 23ms · Sources: EU EUDAMED, US FDA

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PREMIUM PLUS DISPOSABLE PROPHY ANGLE MODEL 3399

FDA 510(k)
FDA Class 1 ·Dental

Bur PM2-70 80K steelØ2.7x80 St

FDA UDI
Bien-Air Surgery SA·17630055512939·

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964057793·Endo Carry-on Procedure Kit includes Suction Tu...

SafeOp

FDA UDI
ALPHATEC SPINE, INC.·00190376331591·SafeOp White Recording Cable (2 Lead)

MAYO-HEGAR NEEDLE HOLDER

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896049871·MAYO-HEGAR NEEDLE HOLDER TUNGSTEN CARBIDE SERRA...

MICRO ANEURYSM CLIP

FDA UDI
SONTEC INSTRUMENTS, INC.·B09921008540·MICRO ANEURYSM CLIP STRAIGHT JAW

BIO-KINETIX® THERMAL NITANIUM®ARCHWIRES

FDA UDI
Ortho Organizers, Inc.·00190707058388·.016 Upper Bio-Kinetix® Thermal Nitanium® Pro F...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450171547·

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197022781·Jako-Type Laryngeal Sickle Knife 295mm,...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197022804·Cotton Carrier 500mm,...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197022798·Cotton Carrier 350mm,...

Monoblock Tibial Trial UC Insert

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215043452·

CHLORINATED POWDER-FREE LATEX EXAMINATION GLOVES, (BLUE, GREEN)

FDA 510(k)
FDA Class 1 ·General Hospital

VIRIDIA INFORMATION CENTER SOFTWARE FOR M3150A AND M3153A, VIRIDIA TELEMETRY SYSTEM TRANSMITTER

FDA 510(k)
FDA Class 2 ·Cardiovascular

Widex

FDA UDI
Widex A/S·05706069727401·Widex EVOKE E-FM (Tech Black S-110 ) RC coil

Widex

FDA UDI
Widex A/S·05706069727807·Widex EVOKE E-FA (Tech Black S-110 ) Telecoil, ...

Widex

FDA UDI
Widex A/S·05706069729801·Widex EVOKE E-FP (Tech Black S-110 ) Telecoil, ...

UNICEL® DXC 600I SYNCHRON® ACCESS CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code MMI·May 8, 2013

SUR-FIT NATURA STOMAHESIVE FLEXIBLE SKIN BARRIER W/PRECUT OPENINGS W45MM (1 3/4"

FDA Adverse Event
Injury ·CONVATEC, INC.·Product code EXE·September 12, 2014

7700

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 12, 2011