FDA UDI In Commercial Distribution 🇺🇸 United States

Diagon

DI: B030MO0012480 · Model: "Bi-Convex, 10mm x 39mm x 18mm, Oblique ASM" · CAMBER SPINE TECHNOLOGIES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Diagon
Primary DI
B030MO0012480
Version / Model
"Bi-Convex, 10mm x 39mm x 18mm, Oblique ASM"
Catalog Number
MO-001-248
Company Name
CAMBER SPINE TECHNOLOGIES, LLC
Labeler DUNS
054205979
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-13
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
39e573ba-4870-4dca-8d46-a613b55c3c00

Device Description

"Bi-Convex, 10mm x 39mm x 18mm, Oblique ASM"

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
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

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary B030MO0012480

Customer Contacts