DYNAMIC TIBIAL NAIL 800512270

GUDID 00887868032639

Biomet Orthopedics, LLC

Tibia nail, sterile

• Primary Device ID: 00887868032639
• NIH Device Record Key: 375cf223-2a56-49c0-b2c6-87cdb4602fbf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DYNAMIC TIBIAL NAIL
• Version Model Number: 8005-12-270
• Catalog Number: 800512270
• 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	00887868032639 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K972183

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 [DYNAMIC TIBIAL NAIL]

• 00887868032837: 8005-13-420
• 00887868032820: 8005-13-405
• 00887868032813: 8005-13-390
• 00887868032806: 8005-13-375
• 00887868032790: 8005-13-360
• 00887868032783: 8005-13-345
• 00887868032776: 8005-13-330
• 00887868032769: 8005-13-315
• 00887868032752: 8005-13-300
• 00887868032745: 8005-13-285
• 00887868032738: 8005-12-420
• 00887868032721: 8005-12-405
• 00887868032714: 8005-12-390
• 00887868032707: 8005-12-375
• 00887868032691: 8005-12-360
• 00887868032684: 8005-12-345
• 00887868032677: 8005-12-330
• 00887868032660: 8005-12-315
• 00887868032653: 8005-12-300
• 00887868032646: 8005-12-285
• 00887868032639: 8005-12-270
• 00887868032622: 8005-11-420
• 00887868032615: 8005-11-405
• 00887868032608: 8005-11-390
• 00887868032592: 8005-11-375
• 00887868032585: 8005-11-360
• 00887868032578: 8005-11-345
• 00887868032561: 8005-11-330
• 00887868032554: 8005-11-315
• 00887868032547: 8005-11-300
• 00887868032530: 8005-11-285
• 00887868032523: 8005-11-270
• 00887868032516: 8005-10-420
• 00887868032509: 8005-10-405
• 00887868032493: 8005-10-390
• 00887868032486: 8005-10-375
• 00887868032479: 8005-10-360
• 00887868032462: 8005-10-345
• 00887868032455: 8005-10-330
• 00887868032448: 8005-10-315
• 00887868032431: 8005-10-300
• 00887868032424: 8005-10-285
• 00887868032417: 8005-10-270
• 00887868032400: 8005-10-255
• 00887868032394: 8005-09-420
• 00887868032387: 8005-09-405
• 00887868032370: 8005-09-390
• 00887868032363: 8005-09-375
• 00887868032356: 8005-09-360
• 00887868032349: 8005-09-345