PS CONSTRAINED INSERT XLG 178902

GUDID 08428898186200

BIOMET SPAIN ORTHOPAEDICS SL

Tibial insert

• Primary Device ID: 08428898186200
• NIH Device Record Key: a0efa5c5-81fe-45d9-bf43-8765a1312c78
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PS CONSTRAINED INSERT XLG
• Version Model Number: 178902
• Catalog Number: 178902
• Company DUNS: 460900553
• Company Name: BIOMET SPAIN ORTHOPAEDICS SL
• 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)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@zimmerbiomet.com
• Phone: +1(800)342-5454
• Email: 3iPBG-CS@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 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	08428898186200 [Primary]

FDA Product Code

• JWH: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

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: 2022-03-10
• Device Publish Date: 2016-03-11

On-Brand Devices [PS CONSTRAINED INSERT XLG]

• 08428898186231: 178912
• 08428898186224: 178908
• 08428898186217: 178905
• 08428898186200: 178902
• 08428898186194: 178900