FDA UDI In Commercial Distribution 🇺🇸 United States

Artemis Proximal Femoral Nail System

DI: 18400659000823 · Model: T6-0300-095S · Glw, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Artemis Proximal Femoral Nail System
Primary DI
18400659000823
Version / Model
T6-0300-095S
Catalog Number
T6-0300-095S
Company Name
Glw, Inc.
Labeler DUNS
081102081
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-30
Public Version
2
Public Version Date
2026-03-12
Public Version Status
Update
Public Device Record Key
a18fc690-2738-42b9-a26e-1fcc1373b539

Device Description

ARTEMIS nail PF, Locking Screw, ø5 x 95

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 18400659000823

Premarket Submissions

Submission Number Supplement Number
K201379 000