LineLogic™

GUDID 10851780008000

Wearable percutaneous catheter/tube holder

Primary Device ID	10851780008000
NIH Device Record Key	520cfc4d-cf40-40aa-9abd-646a6a632949
Commercial Distribution Status	In Commercial Distribution
Brand Name	LineLogic™
Version Model Number	LL-M-6
Company DUNS	070849038
Company Name	SMD Manufacturing LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00851780008003 [Primary]
GS1	10851780008000 [Package] Contains: 00851780008003 Package: Box [10 Units] In Commercial Distribution
GS1	20851780008007 [Package] Package: Case [2 Units] In Commercial Distribution
GS1	30851780008004 [Package] Contains: 20851780008007 Package: Overshipper [16 Units] In Commercial Distribution

KMK	Device, Intravascular Catheter Securement

Steralize Prior To Use	false
Device Is Sterile	true

10851780008208	Sterile, Linelogic™ 8.5 Fr Catheter Stabilization Device
10851780008109	Sterile, Linelogic™ 7 Fr Catheter Stabilization Device
10851780008000	Sterile, Linelogic™ 6 Fr Catheter Stabilization Device