HUMERAL NAIL 800307020

GUDID 00887868031489

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: 00887868031489
• NIH Device Record Key: 04b074ed-9fb5-4d4f-bd64-1eac6d7a60d1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HUMERAL NAIL
• Version Model Number: 8003-07-020
• Catalog Number: 800307020
• 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	00887868031489 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K934643

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 [HUMERAL NAIL]

• 00887868005053: 1709-32
• 00887868005046: 1709-30
• 00887868005039: 1709-28
• 00887868005022: 1709-26
• 00887868005015: 1709-24
• 00887868005008: 1709-22
• 00887868004995: 1709-20
• 00887868004988: 1709-18
• 00887868004971: 1709-16
• 00887868004964: 1708-30
• 00887868004957: 1708-28
• 00887868004940: 1708-26
• 00887868004933: 1708-24
• 00887868004926: 1708-22
• 00887868004919: 1708-20
• 00887868004902: 1708-18
• 00887868004896: 1708-16
• 00887868004889: 1707-30
• 00887868004872: 1707-28
• 00887868004865: 1707-26
• 00887868004858: 1707-24
• 00887868004841: 1707-22
• 00887868004834: 1707-20
• 00887868004827: 1707-18
• 00887868031656: 8003-09-030
• 00887868031649: 8003-09-028
• 00887868031632: 8003-09-026
• 00887868031625: 8003-09-024
• 00887868031618: 8003-09-022
• 00887868031601: 8003-09-020
• 00887868031595: 8003-08-030
• 00887868031588: 8003-08-028
• 00887868031571: 8003-08-026
• 00887868031564: 8003-08-024
• 00887868031557: 8003-08-022
• 00887868031540: 8003-08-020
• 00887868031533: 8003-07-030
• 00887868031526: 8003-07-028
• 00887868031519: 8003-07-026
• 00887868031502: 8003-07-024
• 00887868031496: 8003-07-022
• 00887868031489: 8003-07-020