FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00889095206975 · Model: 6138.1370 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00889095206975
Version / Model
6138.1370
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-16
Public Version
4
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
447c740b-c751-44a9-8d10-53cfd5b204c0

Device Description

70mm Blade, Microtooth - Tapered

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
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00889095206975

Customer Contacts

Device Sizes

Type Value Unit Text
Length 70 Millimeter