132 results · 21ms · Sources: EU EUDAMED, US FDA

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ESOFLIP ES

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

15MM FLEXTUBE BREATHING SYSTEM WITH LUER ELBOW. 1.6M

FDA UDI
Intersurgical Incorporated·05030267062935·15MM FLEXTUBE BREATHING SYSTEM WITH LUER ELBOW....

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756614313·Knee Immobilizer

EXPERT - Joint Fixation System

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258642536·EXPERT Knotless Dual Round Plate Ø6.5mm (2un) R...

LACTOSORB® SYSTEM

FDA UDI
BIOMET MICROFIXATION, INC·00841036053802·

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702435573·Elvarex Forte 3/Thigh High/Slant-Open Toe-Eleph...

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702472790·E3/AG/OT-E/NOP-I-OH/BLU

Electro Lavage

FDA UDI
MECTRA LABS, INC.·00817984010587·Electro Lavage Needle Dual Spike

SureCore Semi-automatic Disposable Biopsy Needle

FDA UDI
Canyon Medical Inc.·06954414666151·Semi-automatic Disposable Biopsy Needle

SureCore Semi-automatic Disposable Biopsy Needle

FDA UDI
Canyon Medical Inc.·06954414666168·Semi-automatic Disposable Biopsy Needle

SureCore Semi-automatic Disposable Biopsy Needle

FDA UDI
Canyon Medical Inc.·06954414666175·Semi-automatic Disposable Biopsy Needle

IMAGYS

FDA 510(k)
FDA Class 2 ·Radiology

MODIFIED MSQ FAMILY OF LOVELY LIGHT/LASER SYSTEMS

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

CLOSER - TSL6

FDA Adverse Event
Injury ·PERCLOSE, INC.·Product code MGB·January 24, 2000

BD ULTRA-FINE 3/10CC INSULIN SYRINGE

FDA Adverse Event
Injury ·BECTON DICKINSON·Product code FMF·March 1, 2000

HOMECHOICE AUTOMATED PD SET W/CASSETTE 4-PRONG

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORP·Product code FKX·May 12, 2000

VASCO TIP BI 9/56

FDA Adverse Event
Injury ·VASCOMED MEDICAL CORP·Product code DTB·April 25, 2000

AVECOR CARDIOVASCULAR INC.

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DWF·November 12, 1999

SNAP LOCK MACROPORT INFUSE-A-PORT SYSTEM

FDA Adverse Event
Other ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·March 1, 2000

NORTH AMERICAN DRAGER

FDA Adverse Event
Malfunction ·NELLCOR PURITAN BENNETT·Product code DQA·April 12, 2000