FDA UDI Not in Commercial Distribution 🇺🇸 United States

JULIET ® Ti OL

DI: 07640151094072 · Model: JUT-OX 28 16-S · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JULIET ® Ti OL
Primary DI
07640151094072
Version / Model
JUT-OX 28 16-S
Catalog Number
JUT-OX 28 16-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-29
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
6e6ae95a-5c95-46ce-a938-3317581b12aa
Distribution End Date
2019-02-05

Device Description

LUMBAR POSTERIOR Ti CAGE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 07640151094072

Device Sizes

Type Value Unit Text
Height 16 Millimeter
Width 10.5 Millimeter
Length 28 Millimeter
Angle 12 degree

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius