BENDING IRON 824129000

GUDID 00887868048876

Biomet Orthopedics, LLC

Manual orthopaedic bender, reusable

• Primary Device ID: 00887868048876
• NIH Device Record Key: 26ded8bb-bf58-472b-9999-536e99015b24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BENDING IRON
• Version Model Number: 8241-29-000
• Catalog Number: 824129000
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• 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

Customer Support Contacts

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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868048876 [Primary]

FDA Product Code

• HXP: INSTRUMENT, BENDING OR CONTOURING

Sterilization

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

[00887868048876]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-11-19
• Device Publish Date: 2018-10-19

On-Brand Devices [BENDING IRON]

• 00887868048876: 8241-29-000
• 00887868446405: 8241-29-000