57 results · 20ms · Sources: EU EUDAMED, US FDA

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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