FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00849044042108 · Model: 675.151 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00849044042108
Version / Model
675.151
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-20
Public Version
3
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
f159ea14-046b-4786-991a-6456f90d2c64

Device Description

Box Curette, Bayonetted, Up Angled, Wide

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
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00849044042108

Customer Contacts

Device Sizes

Type Value Unit Text
Width 15 Millimeter