ProLift Instruments 2019-0016

GUDID 00190837032272

Metallic spinal interbody fusion cage

Primary Device ID	00190837032272
NIH Device Record Key	a2b5909e-8c3e-4dc8-a6d6-f8ce654d87ab
Commercial Distribution Status	In Commercial Distribution
Brand Name	ProLift Instruments
Version Model Number	2019-0016
Catalog Number	2019-0016
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	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
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	00190837032272 [Primary]

MAX	Intervertebral fusion device with bone graft, lumbar

Steralize Prior To Use	true
Device Is Sterile	false

[00190837032272]

Moist Heat or Steam Sterilization