JULIET® Ti JUT-IN 08 10-N

GUDID 07640332470039

TRIAL IMPLANT TI PO/OL SMALL WIDTH L36 W8.5 H10

SpineArt SA

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Primary Device ID	07640332470039
NIH Device Record Key	d14d5a5c-56c4-4bd0-af70-460561d0b879
Commercial Distribution Status	In Commercial Distribution
Brand Name	JULIET® Ti
Version Model Number	JUT-IN 08 10-N
Catalog Number	JUT-IN 08 10-N
Company DUNS	483016148
Company Name	SpineArt SA
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	true
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 Dimensions

Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter
Height	10 Millimeter
Weight	85 Milligram
Length	36 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640332470039 [Primary]

FDA Product Code

HWT

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