VERSANAIL®UNIVERSAL HUMERAL NAIL 181709241

GUDID 00887868021817

Biomet Orthopedics, LLC

Humerus nail, sterile Humerus nail Humerus nail Humerus nail Humerus nail Humerus nail Humerus nail Humerus nail Humerus nail

• Primary Device ID: 00887868021817
• NIH Device Record Key: aec62a52-05cf-4283-8085-d2952b0615bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VERSANAIL®UNIVERSAL HUMERAL NAIL
• Version Model Number: 1817-09-241
• Catalog Number: 181709241
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868021817 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K033329

FDA Product Code

• HSB: ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

On-Brand Devices [VERSANAIL®UNIVERSAL HUMERAL NAIL]

• 00887868021848: 1817-09-301
• 00887868021831: 1817-09-281
• 00887868021824: 1817-09-261
• 00887868021817: 1817-09-241
• 00887868021800: 1817-09-221
• 00887868021794: 1817-09-201
• 00887868021787: 1817-09-181
• 00887868021770: 1817-09-161
• 00887868021763: 1817-08-301
• 00887868021756: 1817-08-281
• 00887868021749: 1817-08-261
• 00887868021732: 1817-08-241
• 00887868021725: 1817-08-221
• 00887868021718: 1817-08-201
• 00887868021701: 1817-08-181
• 00887868021695: 1817-08-161
• 00887868021688: 1817-07-301
• 00887868021671: 1817-07-281
• 00887868021664: 1817-07-261
• 00887868021657: 1817-07-241
• 00887868021640: 1817-07-221
• 00887868021633: 1817-07-201
• 00887868021626: 1817-07-181
• 00887868021619: 1817-07-161