69 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) CONTROLS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
8000230
FDA UDI
LASER PERIPHERALS, LLC·00816469021339·365u Laser Fiber PL
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950016679·CURETTE ANTRALPLASTY CLEPPER TATUM #1 6-1/2" 16...
Silverbolt/Mainframe
FDA UDI
Choice Spine, LP·10885862161055·
PedCAT
FDA UDI
CURVEBEAM, LLC·00863152000317·Cone Beam Computed Tomography diagnostic imagin...
CURE ACP
FDA UDI
SpineArt SA·07640270064475·ANTERIOR CERVICAL PLATE, 2 LEVELS L30
CarboJet® CO2 Bone Lavage System
FDA UDI
Kinamed, Inc.·00898142001494·Wide Angle Nozzle
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700002300·
CURE IVIEW
FDA UDI
MEDITECH SPINE, LLC·B167900002300·
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C2520002300·Curved Ti Rod, 230mm
HARDYDISK, NALIDIXIC ACID, 30MCG
FDA 510(k)
FDA Class 2
·Microbiology
SONOACE 600 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
CS100 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·December 27, 2025
OPEL-L
FDA UDI
SpineArt SA·07640332477571·OPEL-L IVIEW PLATE ASSEMBLY, L30
CURE 2.0 ACP
FDA UDI
SpineArt SA·07640375230980·CERVICAL 2 LEVEL TEMPLATE L30
CURE IVIEW
FDA UDI
MEDITECH SPINE, LLC·B167S1900002300·
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700002300·
CURE 2.0 ACP
FDA UDI
SpineArt SA·07640375232588·ANTERIOR CERVICAL PLATE, 2 LEVELS L30
CS100 INTRA-AORTIC BALLOON PUMP, REFURBISHED, ENGLISH,NON-UTS,INTL
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·December 4, 2025
SERVO I
FDA Adverse Event
Malfunction
·SERVOCARE SYSTEMS AB·Product code CBK·November 18, 2003