FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00193982487393 · Model: 6257.1044 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00193982487393
Version / Model
6257.1044
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-28
Public Version
1
Public Version Date
2023-04-05
Public Version Status
New
Public Device Record Key
b7046595-3e0f-4977-9c22-f9468532b4f7

Device Description

Nail Connection Bolt Driver, Shaft

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
No
PM Exempt
Yes
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
LXH Orthopedic manual surgical instrument

GMDN Terms

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

Identifiers

Type ID
Primary 00193982487393