FDA UDI In Commercial Distribution 🇺🇸 United States

COALITION

DI: 00889095175554 · Model: 6128.4110 · GLOBUS MEDICAL, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COALITION
Primary DI
00889095175554
Version / Model
6128.4110
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-05
Public Version
1
Public Version Date
2019-12-13
Public Version Status
New
Public Device Record Key
d030e01d-d45a-4868-b67a-e9017b7710a2

Device Description

Midline Holding Tip, Large, 10mm

Device Characteristics

Single Use
No
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
Yes
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
OVE Intervertebral fusion device with integrated fixation, cervical
ODP Intervertebral fusion device with bone graft, cervical
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00889095175554

Device Sizes

Type Value Unit Text
Height 10 Millimeter