AccessGUDID - DEVICE: Apex (05391529583309)

GUDID

Device Identifier (DI) Information

Brand Name: Apex
Version or Model: F01-145420
Commercial Distribution Status: In Commercial Distribution
Catalog Number: F01-145420
Company Name: ORTHOXEL DESIGNATED ACTIVITY COMPANY

Primary DI Number: 05391529583309
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 985596830 *Terms of Use

Device Description: Apex Femoral Nail PF Left Ø 14.5 x 420mm

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
33187	Femur intramedullary nail	A rigid rod made of metal or other material intended to be implanted into the intramedullary canal of the femur to immobilize the ends of a fractured bone in position to promote healing; it is not dedicated to extension beyond the joint to an adjacent bone (i.e., not dedicated to arthrodesis/joint fusion). It may be a locked or unlocked model and may include components to assist fixation of more proximal or distal conditions. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
HSB	Rod, Fixation, Intramedullary And Accessories

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Ambient Storage and Handling

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Ø 14.5 x 420mm

Device Record Status

Public Device Record Key: 63e1d394-68c2-498e-8094-b25e069b11da
Public Version Date: February 06, 2025
Public Version Number: 3
DI Record Publish Date: August 12, 2022