40 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ILLUMIGENE C. DIFFICILE, ILLUMIPRO-10 AND ILLUMIGENE C. DIFFICILE EXTERNAL CONTROL KIT, MODELS 280050, 610172, 279920
FDA 510(k)
FDA Class 1
·Microbiology
Bur PM2-95 80K MstickD Ø1.8 St
FDA UDI
Bien-Air Surgery SA·17630055514940·
ILIZAROV
FDA UDI
Smith & Nephew, Inc.·03596010029744·4 HOLE PLATE TO HALF
...
GEN4 INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828159296·GEN4 INTERACTIVE
V.A.T.S. CLASSIC CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921008180·V.A.T.S. CLASSIC CLAMP WITH RATCHET DEBAKEY JAW...
V.A.T.S. CLASSIC CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896003545·V.A.T.S. CLASSIC CLAMP WITH RATCHET DEBAKEY JAW...
INFANT LIMB HOLDER, MODELS 306080 & 306081
FDA 510(k)
FDA Class 1
·General Hospital
BIATAIN AGFOAM DRESSINGS-NON-ADHESIV: 5X7CM, 10X10CM, 10X20CM,15X15CM & 20X20CM
FDA 510(k)
FDA Unclassified
·Unknown
MAXCUT DIAMOND BURS (6/pk) MED 818-052
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D778100818521·MAXCUT DIAMOND BURS (6/pk) Shape: Wheel; Size (...
N/A
FDA UDI
Doppkon GmbH & Co. KG·04262494463716·Curette straight
D 4.5mm, L 7mm, WL 120mm
MAXCUT DIAMOND BURS (6/pk) MED 818-040
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D778100818401·MAXCUT DIAMOND BURS (6/pk) Shape: Wheel; Size (...
MAXCUT DIAMOND BURS (6/pk) MED 818-029
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D778100818291·MAXCUT DIAMOND BURS (6/pk) Shape: Wheel; Size (...
REMSTAR PRO C-FLEX+
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·January 29, 2025
Widex
FDA UDI
Widex A/S·05706069727258·Widex EVOKE E-FM (Summer gold S-220 ) RC coil
Widex
FDA UDI
Widex A/S·05706069727654·Widex EVOKE E-FA (Summer gold S-220 ) Telecoil,...
Widex
FDA UDI
Widex A/S·05706069729658·Widex EVOKE E-FP (Summer gold S-220 ) Telecoil,...
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 30, 2024
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·January 24, 2022
VELA VENTILATOR
FDA Adverse Event
Injury
·VYAIRE MEDICAL·Product code CBK·August 27, 2020
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 12, 2011