315 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Wedge Microcatheter
FDA 510(k)
FDA Class 2
·Cardiovascular
BRUSIO 2.5mm Flex Straight Plate, 14 Hole
FDA UDI
Bonebridge AG·07640187463248·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694027007·2.0mm X 14mm Cannulated Headless Screw
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613085087·Sideport Knife, Angled, 1.4mm, 6 Per Box
LVIS Jr.
FDA UDI
Microvention, Inc.·00842429100806·Stent
LVIS Jr.
FDA UDI
Microvention, Inc.·00810170018978·Stent
LVIS Jr.
FDA UDI
Microvention, Inc.·00812636020136·Stent
HORICO
FDA UDI
Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1720142·Rotary Diamond Instrument
HORICO
FDA UDI
Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1720145·Rotary diamond instrument
VITASCORE
FDA 510(k)
FDA Class 2
·Anesthesiology
TENS STIMULATOR, MODELS 2800 AND 3000
FDA 510(k)
FDA Class 2
·Neurology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694068444·Cannulated 2.0 x 14mm Headless Screw Sterile Qty 5
PUSHING CATHETER
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 19, 2022
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013
INFUSOMAT SPACE
FDA Adverse Event
Malfunction
·B. BRAUN·Product code FRN·July 12, 2011
ABBOTT VASCULAR
FDA Adverse Event
Injury
·ABBOTT LABS·Product code DQX·September 23, 2008
ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020
ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020
FILIFORM DOUBLE PIGTAIL URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·June 30, 2022
PUSHING CATHETER
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·September 15, 2023