Home GUDID 20609271247424 DARCO® Toe Cap
Primary DI 20609271247424
Brand DARCO® Toe Cap
Company DARCO INTERNATIONAL, INC.
Model TCDBM3
Catalog number TCDBM3
Device description ML Black for Relief Dual®
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 FMP Protector, skin pressure
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class FMP Protector, Skin Pressure General Hospital 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20609271247424 Package GS1 50 In Commercial Distribution 00609271247420 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 20609271247424 20609271247424 00609271247420 00609271247420 609271247420 0609271247420
GMDN Terms# Term, Definition table Term Definition Foot friction/impact protector A device designed to be worn over/on the foot, often while wearing shoes, to provide a cushion to protect the whole foot or parts of the foot (e.g., toes, metatarsal heads, heel) from friction against surfaces or knocks against objects, to relieve pain during walking, and/or to prevent formation of hard areas and callouses. It is typically made of soft-padded or gel materials in a variety of forms (e.g., strip, pad, elastic band, digital tube), and some types may be inflatable or held in place with bands or straps around the foot. It is not specifically designed to protect a bunion. 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
Other Devices Sharing Product Codes#