FDA UDI In Commercial Distribution 🇺🇸 United States

Artemis Proximal Femoral Nail System

DI: 18400659000274 · Model: T5-0320-000 · 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
18400659000274
Version / Model
T5-0320-000
Catalog Number
T5-0320-000
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
7a0aea0b-1f93-479c-b66c-1c45c5a8dc56

Device Description

ARTEMIS nail PF, Locking Screw Guide Sleeve

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Primary 18400659000274