Luther Needlesafe Products 20175001

GUDID 10850017259024

Peripheral intravenous cannula

Primary Device ID	10850017259024
NIH Device Record Key	40b329c7-cd3c-4f49-9c36-07e7667fab7d
Commercial Distribution Status	In Commercial Distribution
Brand Name	Luther Needlesafe Products
Version Model Number	20175001
Catalog Number	20175001
Company DUNS	117440613
Company Name	Luther Needlesafe Products, LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00850017259027 [Primary]
GS1	10850017259024 [Package] Contains: 00850017259027 Package: Inner Box [50 Units] In Commercial Distribution

FOZ	Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

Steralize Prior To Use	false
Device Is Sterile	true

00850017259058	Mini-Midline Extended Dwell Peripheral Catheter - 24Ga, 1.25”
10850017259048	Mini-Midline Extended Dwell Peripheral Catheter - 22Ga, 1.75”
10850017259031	Mini-Midline Extended Dwell Peripheral Catheter - 22Ga, 1.50”
10850017259024	Mini-Midline Extended Dwell Peripheral Catheter - 20Ga, 1.75”
10850017259017	Mini-Midline Extended Dwell Peripheral Catheter - 20Ga, 1.50”
10850017259000	Mini-Midline Extended Dwell Peripheral Catheter - 18Ga, 1.75”