FDA UDI In Commercial Distribution 🇺🇸 United States

SUSTAIN

DI: 00849044077490 · Model: 304.313 · GLOBUS MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SUSTAIN
Primary DI
00849044077490
Version / Model
304.313
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-06
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
1c0777ae-f09d-45c0-bf10-e47569646224

Device Description

SUSTAIN Radiolucent Spacer, Large, Anterior, 13mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00849044077490

Customer Contacts

Device Sizes

Type Value Unit Text
Height 13 Millimeter
Depth 31 Millimeter
Width 25 Millimeter