36 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Software Option For Anesthesia Gas Machine To Achieve And Maintain Targeted End Tidal Oxygen And Anesthetic Agents
FDA Pre-Market Approval
FDA Class 3
·Et Control
NuVasive
FDA UDI
Nuvasive, Inc.·00195377106070·NTS Dilator, 18mm
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319744062·Fomon Nasal Knife 6" (15.2 cm), double ended, ...
Admiral
FDA UDI
Seaspine Orthopedics Corporation·10889981278069·Cervical Plate, 2 Level, 18mm
Bard Stinger Ablation Catheter: Item Numbers 210001 218501 L210001 210002 218502 L210002 210003 218503 L210003 210004 218504 L210004 210005 218505 L210005 210006 218506 L210006 210007 218507 L210007 210015 218516 L210008 210016 218518 L210009 210017 218519 L210010 210018 218520 L210011 210019 218521 L210012 210020 218523 L210013 210023 218524 L210014 210024 218525 L210015 210025 218526 L210016 210026 218527 L210017 210027 218528 L210018 210028 218529 210029 210030
FDA Recall
Terminated
·C. R.Bard, Inc./Electrophysiology Division·January 8, 2003
Anatomic Healing Cap 2mm Wide
FDA UDI
NOGA MEDICAL PRODUCTS LTD·07290118142881·Anatomic Healing Cap 2mm Wide
Multi-Unit H3mm
FDA UDI
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011628·
Multi-Unit H3mm
FDA UDI
NOGA MEDICAL PRODUCTS LTD·07290118143154·Multi-Unit H3mm
TriplePlay
FDA UDI
DYMEDIX DIAGNOSTICS, INC.·00817377020919·FM1 - Grael
NA
FDA UDI
STRYKER CORPORATION·04546540144195·Fan Spray Tip
BINAXNOW COVID-19 AG SELF TEST 2CT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·March 28, 2023
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·SHARPS TERMINATOR
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT(TM) CK SYSTEM
Disposable Medical Mask
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 22, 2024
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 5, 2025
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CONDUCTIVE KERATOPLASTY SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM