76 results · 24ms · Sources: EU EUDAMED, US FDA

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COMPRESSOR NEBULIZER MODEL MCN-S600XX

FDA 510(k)
FDA Class 2 ·Anesthesiology

Protective Cap

FDA UDI
BIO CONCEPT Co., Ltd.·06947600303695·

RUSCH

FDA UDI
TELEFLEX INCORPORATED·04026704300761·Nasopharyngeal Airway (Amber)

Trimedyne® 1230-30 OmniPulse Jr.™ Holmium Laser System

FDA UDI
TRIMEDYNE, INC.·M4731230300·Model 1230-30 - OmniPulse Jr. Holmium Laser System

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587A123030120·12mm H x 30mm W x 30mm L x 12 degrees ALIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587A12303080·12mm H x 30mm W x 30mm L x 8 degrees ALIF

EXPERT - Flexible Joint Fixation System

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258661933·EXPERT FAST- AC - Flexible Knotless Fixator Acr...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587A123030150·12mm H x 30mm W x 30mm L x 15 degrees ALIF

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K1230000·Rod Holder, Curved, 5.5 mm

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197413473·CERA-CUT® Mayo Scissors straig...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197413466·CERA-CUT® Mayo Scissors curved...

DEMETECH POLYESTER NONABSORBABLE SUTURE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SPINEOLOGY PEEK BULLET LUMBAR INTERBODY FUSION DEVICE

FDA 510(k)
FDA Class 2 ·Orthopedic

Ideal Eyes

FDA UDI
STRYKER CORPORATION·07613327062328·Arthroscope, Autoclavable, J-Lock, 30 ¿ View Di...

RMNIPULSE HOLMIUM LASER SYSTEM/1210; MAX/1210-VHP; JR. 1230-30; N/A 1500-A

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 22, 2024

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
Malfunction ·INVAMEX·Product code IOR·May 21, 2013

RESERVOIR 3ML

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code FRN·September 26, 2014

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 14, 2011

PENUMBRA SMART COIL

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code HCG·December 11, 2015