Home GUDID 10850017259031 Luther Needlesafe Products
Primary DI 10850017259031
Brand Luther Needlesafe Products
Company Luther Needlesafe Products, LLC
Model 22150001
Catalog number 22150001
Device description Mini-Midline Extended Dwell Peripheral Catheter - 22Ga, 1.50”
Published 2023-05-01
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days General Hospital 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10850017259031 Package GS1 50 In Commercial Distribution 00850017259034 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 10850017259031 10850017259031 00850017259034 00850017259034 850017259034 0850017259034
GMDN Terms# Term, Definition table Term Definition Peripheral intravenous cannula A short, thin tube intended to be inserted into a peripheral vein (typically on the hand/arm) to enable short-term (< 30 days) intravenous (IV) access for administration of fluids/medication and blood sampling. Also referred to as a peripheral IV catheter, it is typically assembled with a dedicated introduction needle, and usually includes connectors, injection ports, and wings for fixation. It is not intended to be advanced to the central vasculature. This is a single-use device.
Regulatory Flags# DUNS number 117440613 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true 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 00850017259003 Luther Needlesafe Products 18175001 18175001 2023-05-01 00850017259010 Luther Needlesafe Products 20150001 20150001 2023-05-01 00850017259027 Luther Needlesafe Products 20175001 20175001 2023-05-01 00850017259034 Luther Needlesafe Products 22150001 22150001 2023-05-01 00850017259041 Luther Needlesafe Products 22175001 22175001 2023-05-01 00850017259058 Luther Needlesafe Products 24125001 24125001 2023-05-01 10850017259000 Luther Needlesafe Products 18175001 18175001 2023-05-01 10850017259017 Luther Needlesafe Products 20150001 20150001 2023-05-01 10850017259024 Luther Needlesafe Products 20175001 20175001 2023-05-01 10850017259048 Luther Needlesafe Products 22175001 22175001 2023-05-01
Other Devices Sharing Product Codes#