TruLift Lateral

GUDID 00190837153410

Metallic spinal interbody fusion cage

Primary Device ID	00190837153410
NIH Device Record Key	304ddac5-73d2-4c04-84af-c0f8a65ad464
Commercial Distribution Status	In Commercial Distribution
Brand Name	TruLift Lateral
Version Model Number	68-1850-0708
Company DUNS	183641617
Company Name	Life Spine, Inc.
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	false
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	00190837153410 [Primary]

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar

Steralize Prior To Use	false
Device Is Sterile	true