FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00193982071271 · Model: 6147.2209 · GLOBUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00193982071271
Version / Model
6147.2209
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-27
Public Version
1
Public Version Date
2019-07-05
Public Version Status
New
Public Device Record Key
d2b64016-1d33-4e79-b622-1f7c6007a768

Device Description

Modular Trial, 14x16mm, 12°, 9mm

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
Yes
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
44788 Spinal implant trial

Identifiers

Type ID
Primary 00193982071271

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Lordosis 12 Degree
Width 16 Millimeter
Depth 14 Millimeter
Height 9 Millimeter