PLIF LITE

GUDID 08057432565692

Metallic spinal interbody fusion cage

Primary Device ID	08057432565692
NIH Device Record Key	59c75077-3f37-4741-a53a-ffe2bf9e1851
Commercial Distribution Status	In Commercial Distribution
Brand Name	PLIF LITE
Version Model Number	LFC-001PK2610
Company DUNS	544150399
Company Name	SINTEA PLUSTEK SRL
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Unsafe
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	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	08057432565692 [Primary]

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar

Steralize Prior To Use	false
Device Is Sterile	true