ACIF

GUDID 07640173166443

Polymeric spinal interbody fusion cage

Primary Device ID	07640173166443
NIH Device Record Key	24253c9d-37ef-4194-a4f5-59847ec7bf0b
Commercial Distribution Status	In Commercial Distribution
Brand Name	ACIF
Version Model Number	053.049
Company DUNS	482467792
Company Name	coLigne AG
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	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	07640173166443 [Primary]

ODP	Intervertebral Fusion Device With Bone Graft, Cervical

Steralize Prior To Use	true
Device Is Sterile	false

[07640173166443]

Moist Heat or Steam Sterilization

Mark Image Registration \| Serial	Company Trademark Application Date
ACIF 79067662 3781331 Live/Registered	EMILCERAMICA S.R.L. 2009-02-19