OPTILOCK PERIARTICULAR PLATING SYSTEM 26490

GUDID 00880304492660

Orthopaedic bone screw, non-bioabsorbable, sterile

Primary Device ID	00880304492660
NIH Device Record Key	5ca32279-26a0-4d5e-88d3-0377829f644a
Commercial Distribution Status	In Commercial Distribution
Brand Name	OPTILOCK PERIARTICULAR PLATING SYSTEM
Version Model Number	26490
Catalog Number	26490
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	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

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

Device Size Text, specify	0
Device Size Text, specify	0

Device Issuing Agency	Device ID
GS1	00880304492660 [Primary]

HRS	PLATE, FIXATION, BONE

Steralize Prior To Use	true
Device Is Sterile	false

[00880304492660]

Moist Heat or Steam Sterilization

[00880304492660]

Moist Heat or Steam Sterilization