132 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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