BEUDAMED
    27 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NY-STA BLACK 2/0 18" (45CM) DS24 VPL

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·May 5, 2026

    SUPRAMID BLACK 3/0 (2) 45CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·June 13, 2022

    DAFILON 3/0 (2) 100M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·December 27, 2023

    SKIN SUTURE PACK DAFILON

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 18, 2024

    SUPRAMID BLACK 4/0 (1.5) 45CM DS16

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 17, 2025

    DAFILON 3/0 (2) 100M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 22, 2025

    SUPRAMID BLACK 4/0 (1.5) 45CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·March 10, 2026

    SUPRAMID BLACK 3/0 (2) 75CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·January 11, 2023

    SUPRAMID BLACK 4/0 (1.5) 45CM DS16

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·June 17, 2022

    SUPRAMID BLACK 4/0 (1.5) 45CM DS16

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·March 9, 2026

    SUPRAMID BLACK 3/0 (2) 75CM DS24

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·February 24, 2026

    SUPRAMID BLACK 4/0 (1.5) 45CM HS15

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·March 24, 2025

    Oticon

    FDA UDI
    Oticon A/S·05707131279897·H33, DESIGNRITE 10 WL CRED

    ProLift Expandable Spacer System

    FDA UDI
    Life Spine, Inc.·00190837065720·

    Statcorp Medical

    FDA UDI
    Statcorp Medical·10841522123528·BP CUFF,TL YLW VNYL,1T,L.ADULT,32-42CM,HP,5/BG

    Statcorp Medical

    FDA UDI
    Statcorp Medical·10841522104633·BP CUFF,TL YLW VNYL,1T,L.ADULT,32-42CM,HP,EA

    PRO-TOE VO HAMMERTOW IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KLS MARTIN STERNAL TALON

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADVANTA V12 VASCULAR STENTS

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL·Product code NIN·October 1, 2018