BEUDAMED
    34 results · 89ms · Sources: EU EUDAMED, US FDA

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    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Suture, Absorbable, Synthetic, Polyglycolic Acid

    FDA Pre-Market Approval
    FDA Class 2 ·PDS(TM) SUTURE (CLEAR)

    Proficient™ Posterior Cervical Spine System

    FDA UDI
    Spine Wave, Inc.·10840642114720·Cannulated, Extended Tab Screw, 4.2 mm x 50 mm

    Proficient™ Posterior Cervical Spine System

    FDA UDI
    Spine Wave, Inc.·10840642120462·Cannulated, Extended Tab Screw, 3.8 mm X 10 mm

    NewPort

    FDA UDI
    Seaspine Orthopedics Corporation·10889981084745·Working Tube 18 x 40mm, Angled Tip

    NUTRIENT MIXTURE F-10 -HAM, N 1387, W/L-GLUTAMINE

    FDA 510(k)
    FDA Class 1 ·Hematology

    REINFORCED DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·ORIGEN BIOMEDICAL, INC.·Product code DWF·November 1, 2017

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·May 18, 2021

    The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel lumen catheter with a wire reinforcement layer on the tip of the device. A thin sheath is used to cover and secure the wire layer and is heat shrunk into a permanent position.

    FDA Recall
    Terminated ·OriGen Biomedical, Inc.·Product code DWF·August 2, 2017

    GREENLIGHT HPS BPH FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·August 5, 2013