Home GUDID 10609271939452 DARCO® Web Ankle Brace
Primary DI 10609271939452
Brand DARCO® Web Ankle Brace
Company DARCO INTERNATIONAL, INC.
Model WB4
Catalog number WB4
Device description XL Black
Published 2023-02-08
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name ITW JOINT, ANKLE, EXTERNAL BRACE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class ITW Joint, Ankle, External Brace Physical Medicine 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10609271939452 Package GS1 12 In Commercial Distribution 20609271939459 Package GS1 36 In Commercial Distribution 00609271939455 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 10609271939452 10609271939452 20609271939459 20609271939459 00609271939455 00609271939455 609271939455 0609271939455
GMDN Terms# Term, Definition table Term Definition Ankle/foot orthosis A prefabricated (non-customized) externally applied and wearable appliance or apparatus intended to encompass the ankle joint, or the ankle and foot, to support, align, prevent, or correct orthopaedic deformities/injuries or to improve function of the ankle and/or foot through actions such as alignment, hinge-support, or dorsiflexion assistance. It may also be intended to offload and redistribute foot pressures that affect pedal circulation to improve blood flow and help heal diabetic foot ulcers or postsurgical wounds, and may include patient adaptable plantar inserts. This is a reusable device.
Regulatory Flags# DUNS number 184231298 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00609271200135 16'' DLX POST-OP KNEE IMMOB 462-0012-30 462-0012-30 2023-02-08 00609271200159 16'' DLX POST-OP KNEE IMMOB 462-0012-40 462-0012-40 2023-02-08 00609271200173 16'' DLX POST-OP KNEE IMMOB 462-0012-50 462-0012-50 2023-02-08 00609271200180 16'' DLX POST-OP KNEE IMMOB 462-0012-60 462-0012-60 2023-02-08 00609271200197 16'' DLX POST-OP KNEE IMMOB 462-0012-70 462-0012-70 2023-02-08 00609271200333 20'' DLX POST-OP KNEE IMMOB 462-0014-30 462-0014-30 2023-02-08 00609271200357 20'' DLX POST-OP KNEE IMMOB 462-0014-40 462-0014-40 2023-02-08 00609271200371 20'' DLX POST-OP KNEE IMMOB 462-0014-50 462-0014-50 2023-02-08 00609271200388 20'' DLX POST-OP KNEE IMMOB 462-0014-60 462-0014-60 2023-02-08 00609271200395 20'' DLX POST-OP KNEE IMMOB 462-0014-70 462-0014-70 2023-02-08 00609271210509 20'' DLX 3-PANEL KNEE IMMOB 462-0025-10 462-0025-10 2023-02-08 00609271210608 20'' DLX 3-PANEL KNEE IMMOB 462-0026-10 462-0026-10 2023-02-08 00609271210806 20'' DLX 3-PANEL KNEE IMMOB 462-0028-10 462-0028-10 2023-02-08 00609271610774 "Knee Immobilizer, Super-Lite, Contoured Stay, 12"" (small)" E59410 E59410 2023-02-08 00609271610781 "Knee Immobilizer, Super-Lite, Contoured Stay, 12"" (medium)" E59411 E59411 2023-02-08 00609271610798 "Knee Immobilizer, Super-Lite, Contoured Stay, 12"" (large)" E59412 E59412 2023-02-08 00609271610804 "Knee Immobilizer, Super-Lite, Contoured Stay, 12"" (x-large)" E59413 E59413 2023-02-08 00609271610811 "Knee Immobilizer, Super-Lite, Contoured Stay, 16"" (small)" E59414 E59414 2023-02-08 00609271610828 "Knee Immobilizer, Super-Lite, Contoured Stay, 16"" (medium)" E59415 E59415 2023-02-08 00609271610835 "Knee Immobilizer, Super-Lite, Contoured Stay, 16"" (large)" E59416 E59416 2023-02-08
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