FDA UDI In Commercial Distribution 🇺🇸 United States

TRANSCONTINENTAL

DI: 00889095219418 · Model: 375.630 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRANSCONTINENTAL
Primary DI
00889095219418
Version / Model
375.630
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
6a725f51-ad7e-4ad2-b7f9-d970c62c414d

Device Description

TransContinental M Spacer 20deg, 20mm x 35mm, 19mm

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

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00889095219418

Customer Contacts

Device Sizes

Type Value Unit Text
Length 35 Millimeter
Height 19 Millimeter
Device Size Text, specify Lordosis 20 Degree
Width 20 Millimeter