BEUDAMED
    20 results · 13ms · Sources: EU EUDAMED, US FDA

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    Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number: 92810 Software Version: 11.6.0 Product Description: Cardiology Information Management System Component: No The Sentinel Cardiology Information Management System is intended to connect to supported medical devices and analyzers in order to download, store, access and manage cardiovascular information and to manage patient and facility information.

    FDA Recall
    Open, Classified ·Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom·Product code DQK·September 16, 2025

    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    Hobbs Posi-Stop Injection Needle Catalog Number: 4718

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·July 29, 2022

    Hobbs Posi-Stop Injection Needle Catalog Number: 4722

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·July 29, 2022

    Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    Hobbs Posi-Stop Injection Needle Catalog Number: 4720

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·July 29, 2022

    ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early-stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device UPN: (1)Twin Pack Box 1 M00519210; (2)Twin Pack Box 10 M00519211; (3)Single Pack Box 10 M00519231

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code FBK·October 10, 2022

    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    injeTAK Adjustable Tip Needles Needle Sheath diameter 6Fr with 35-50cm in length Stainless-stell needle cannula is 25 gauge

    FDA Recall
    Open, Classified ·Labories Medical Technologies·Product code FBK·February 7, 2023

    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·October 4, 2024

    Injection Needle, 3 Fr., REF: 27030N; Injection Cannula, 6 Fr., REF: 27182A

    FDA Recall
    Open, Classified ·Karl Storz Endoscopy·Product code FBK·October 24, 2023

    Hobbs Posi-Stop Injection Needle Catalog Number: 4702

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·July 29, 2022

    Hobbs Posi-Stop Injection Needle Catalog Number: 4712

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·July 29, 2022

    ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps, adenomas, early stage cancers or other gastrointestinal mucosal lesions, prior to excision with a snare or other suitable endoscopic device. UPN (1)ORISE ProKnife 1.5 mm Electrode - Kit M00519380; (2) ORISE ProKnife 2.0 mm Electrode - Kit M00519390; (3) ORISE ProKnife 3.0 mm Electrode - Kit M00519400

    FDA Recall
    Open, Classified ·Boston Scientific Corporation·Product code FBK·October 10, 2022

    Hobbs Posi-Stop Injection Needle Catalog Number: 4704

    FDA Recall
    Open, Classified ·Hobbs Medical, Inc.·Product code FBK·July 29, 2022