IMPIX TLIF B15130615S

GUDID 03613720193807

Polymeric spinal interbody fusion cage

Primary Device ID	03613720193807
NIH Device Record Key	e643bf2d-7d7e-4c48-90de-087134033f3c
Commercial Distribution Status	In Commercial Distribution
Brand Name	IMPIX TLIF
Version Model Number	B15130615S
Catalog Number	B15130615S
Company DUNS	383228632
Company Name	MEDICREA INTERNATIONAL
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	03613720193807 [Primary]

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar

Steralize Prior To Use	false
Device Is Sterile	true