Home GUDID 10609271039800 DARCO® Monofilament Tester
Primary DI 10609271039800
Brand DARCO® Monofilament Tester
Company DARCO INTERNATIONAL, INC.
Model MFT
Catalog number MFT
Device description Universal
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 GXB ESTHESIOMETER
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class GXB Esthesiometer Neurology 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10609271039800 Package GS1 24 In Commercial Distribution 20609271039807 Package GS1 288 In Commercial Distribution 00609271039803 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 10609271039800 10609271039800 20609271039807 20609271039807 00609271039803 00609271039803 609271039803 0609271039803
GMDN Terms# Term, Definition table Term Definition Pressure algometer/aesthesiometer, mechanical A manual, non-powered instrument designed to measure: 1) a patient's sensitivity to pain (pain threshold) by applying a painful, calibrated mechanical force to the skin; and 2) tactile sensibility by application of a thin filament(s) to the skin. It is typically a holder/pen which includes a strain gauge, a pressure algesimeter tip(s), and a thin filament(s) with a pre-set flexibility intended to apply a known pressure (point aesthesiometer). The device is typically used to evaluate the effects of pain after the use of anaesthesia/analgesics and/or during diagnosis or treatment of nerve injuries and neuropathies. This is a reusable device when the consumable products have been replenished.
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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