BEUDAMED
    41 results · 11ms · Sources: EU EUDAMED, US FDA

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    Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-BW1; (2) Arrow Arterial Access Tray with 0.021" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-CK; (3) Arrow Arterial Access Kit, .025 inch dia. spring-wire guide, REF ASK-04001-VAMC1; (4) Arrow Arterial Catheterization Kit, 20 Ga., 4.45 cm catheter length, .018 inch dia. spring-wire guide, REF ASK-04020-BHS; (5) Arrow Arterial Catheterization Kit, 20 Ga., 4.45 cm catheter length, .025 inch dia. spring-wire guide, REF ASK-04020-BID; (6) Arrow Arterial Line Kit, 20 Ga., 12 cm. catheter length, .025 inch dia. spring-wire guide, REF ASK-04020-HMC; (7) Arrow Arterial Catheterization Kit, 20 Ga. 4.45 cm catheter length, .018 inch dia. spring-wire guide, REF ASK-04020-HOA; (8) Arrow Arterial Catheterization Kit, 20 Ga., 4.45 cm. catheter length, .018 inch dia. spring-wire guide, REF ASK-04020-KSD; (9) Arrow Arterial Catheterization Kit, 20 Ga. 4.45 cm catheter length, .018 inch dia. spring-wire guide, REF ASK-04020-LOL; (10) Arrow Radial Catheterization, 20 Ga. 4.45 cm catheter length, .018 inch dia. spring-wire guide, REF ASK-04020-MHS; (11) Arrow Arterial Catheterization Kit, 20 Ga., 4.45 cm catheter length, 018 inch dia. spring-wire guide, REF ASK-04020-MIB3; (12) Arrow Arterial Catheterization Kit, 20 Ga., 4.45 cm catheter length, .018 dia. spring- wire guide, REF ASK-04020-PRH; (13) Arrow Arterial Catheterization Kit, 20 Ga., 4.45 cm catheter length, .018 dia. spring-wire guide, REF ASK-04020-UOIL; (14) Arrow QuickFlash Radial Artery Catheterization Kit, 20 Ga., 3.81 cm catheter length, .018 inch dia. spring-wire guide, REF ASK-04220-KSP; and (15) Arrow Arterial Catheterization Kit, 20 Ga. 4.45/12 cm catheter length, .018 inch dia. spring-wire guide, REF ASK-04500-HFH4.

    FDA Recall
    Open, Classified ·ARROW INTERNATIONAL Inc.·Product code DQX·July 26, 2024

    Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;

    FDA Recall
    Open, Classified ·Stryker GmbH Bohnackerweg 1 Selzach Switzerland·Product code LXH·March 28, 2025

    Guide Wire with Ruler Tube 3x1000 mm DIA; Catalog number/REF: 2351-3100S;

    FDA Recall
    Open, Classified ·Stryker GmbH Bohnackerweg 1 Selzach Switzerland·Product code LXH·March 28, 2025

    Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; mobile patient alarm

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·September 25, 2023

    Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-59360; mobile patient alarm

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·September 25, 2023

    Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·December 8, 2025

    Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·December 8, 2025

    Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireless nurse call station.

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·June 20, 2024

    Arial mobile application, model numbers 54640, 54630, and 54630-SMA, that utilizes Apple iOS 17.4 and Apple iOS 17.5, a component of the Arial Emergency and Nurse Call System.

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·April 11, 2024

    Arial Water Resistant Pendant with Long Wristband, Models: 59362 and 2560-59362; mobile patient alarm

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·September 25, 2023

    Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas to allow immediate staff response.

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·June 20, 2024

    Ascom Telligence Nurse Call System

    FDA Recall
    Open, Classified ·Ascom (US) Inc.·Product code IQA·November 2, 2018

    Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system.

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·February 6, 2023

    Senior Living Arial Emergency and Nurse Call Systems

    FDA Recall
    Open, Classified ·Stanley Security Solutions Inc·Product code IQA·November 17, 2021

    Arial Server Software Versions 11.1.4 through 11.1.6, SKU 54305, in conjunction with the Arial Mobile Application or Arial Care Giver Application

    FDA Recall
    Open, Classified ·Securitas Healthcare LLC·Product code IQA·November 1, 2024

    ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning in Radiation Therapy, Radiology, or Radiology image-guided treatment environment. Part Number: 1SOPT00009

    FDA Recall
    Open, Classified ·LEONI CIA CABLE SYSTEMS 5 avenue Victor Hugo Chartres France·Product code JAI·October 6, 2023

    ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning in Radiation Therapy, Radiology, or Radiology image-guided treatment environment. Part Number: 1SOPT00003

    FDA Recall
    Open, Classified ·LEONI CIA CABLE SYSTEMS 5 avenue Victor Hugo Chartres France·Product code JAI·October 6, 2023

    TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis

    FDA Recall
    Open, Classified ·Grace Medical, Inc.·Product code ETB·April 3, 2026

    Modular Stem cylindrical, Tilastan, press-fit cementless, L= 80 mm, DIA = 11 mm, Product Code: 880-601/11

    FDA Recall
    Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code JWH·February 14, 2025

    Modular Stem cylindrical, Tilastan, press-fit cementless, L= 80 mm, DIA = 13 mm, Product Code: 880-601/13

    FDA Recall
    Open, Classified ·Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany·Product code JWH·February 14, 2025