FDA UDI In Commercial Distribution 🇺🇸 United States

ANTHEM

DI: 00889095614435 · Model: 2187.4718 · GLOBUS MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ANTHEM
Primary DI
00889095614435
Version / Model
2187.4718
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-14
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
d2ec6923-d726-45d7-8c65-d78cf5b4a5fb

Device Description

ANTHEM Lateral Proximal Tibia Plate, Right, 18 Hole, 294mm, SS

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
HWC Screw, fixation, bone
HRS Plate, fixation, bone

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00889095614435

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K173166 000

Device Sizes

Type Value Unit Text
Length 294 Millimeter
Device Size Text, specify 18 Hole
Device Size Text, specify Right