57 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Separator, Automated, Blood Cell And Plasma, Therapeutic
FDA Pre-Market Approval
FDA Unclassified
·THERAPEUTIC APHERESIS SYSTEM
CASE MEDICAL
FDA UDI
Case Medical Inc.·00653159005473·Full Size Lid
Pro Advantage
FDA UDI
NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P8500912·Pro Advantage Electrode 2 Round 4PK
Pro Advantage
FDA UDI
NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P8500902·Pro Advantage Electrode Foam 2X2 4PK
DULBECCO'S MODIFIED EAGLE'S MED. (DME) W/GLUCOSE A
FDA 510(k)
FDA Class 1
·Hematology
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·CHLORHEXIDINE-THIMEROSAL-EDETATE DISODIUM DISINFEC
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·CHLORHEXIDINE-THIMEROSAL-EDETATE DISODIUM DISINFEC
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·UNILENS (HEFILCON A) CONTACT LENS
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·CHLORHEXIDINE-THIMEROSAL-EDETATE DISODIUM DISINFEC
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·SIMULVUE (HEFILCON A) BIFOCAL CONTACT LENS
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·CHLORHEXIDINE-THIMEROSAL-EDETATE DISODIUM DISINFEC
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·CHLORHEXIDINE-THIMEROSAL-EDETATE DISODIUM DISINFEC
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ALGES(TM) (HEFILCON A) CONTACT LENS
SPINALPAK NON-INVASIVE SPINE FUSION STIMULATOR SYSTEM
FDA Adverse Event
Injury
·EBI, LLC.·Product code LOF·May 9, 2017
STIMULATOR, BONE GROWTH, NON-INVASIVE
FDA Adverse Event
Injury
·EBI, LLC.·Product code LOF·October 11, 2017