AccessGUDID - DEVICE: VERSANAIL®UNIVERSAL FEMORAL NAIL (00887868019371)

GUDID

Device Identifier (DI) Information

Brand Name: VERSANAIL®UNIVERSAL FEMORAL NAIL
Version or Model: 1813-08-500
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 181308500
Company Name: Biomet Orthopedics, LLC

Primary DI Number: 00887868019371
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 129278169 *Terms of Use

Device Description: No description.

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?
56643	Femur nail, non-sterile	A non-sterile rod made of metal or other material which, when inserted into the intramedullary canal of the femur, acts to immobilize by holding the ends of a fractured bone in position to promote healing. The device may also be used to support the bone in the presence of a pathological condition, or for knee arthrodesis. The device may be a locked or unlocked model, and possess components to assist fixation of more proximal or distal conditions. This is a single-use device intended to be sterilized prior to use.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
HRS	PLATE, FIXATION, BONE
HTY	PIN, FIXATION, SMOOTH
HTN	WASHER, BOLT NUT
JDW	PIN, FIXATION, THREADED
HSB	ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
LXT	APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE
KTT	APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
HWC	Screw, fixation, bone

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: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 8MM X 50CM

Device Record Status

Public Device Record Key: b83c947d-2de3-47a8-9347-8398f9bf3d7f
Public Version Date: October 24, 2022
Public Version Number: 4
DI Record Publish Date: October 24, 2015