Bio-Modular® Choice Instruments 406802

GUDID 00887868505256

Biomet Orthopedics, LLC

Surgical instrument handle, non-torque-limiting

• Primary Device ID: 00887868505256
• NIH Device Record Key: 62a40a2a-64c2-483f-9ccb-4b4515eb83c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bio-Modular® Choice Instruments
• Version Model Number: 406802
• Catalog Number: 406802
• 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
• 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
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00887868505256 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

[00887868505256]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-10
• Device Publish Date: 2021-04-30

On-Brand Devices [Bio-Modular® Choice Instruments]

• 00880304447820: 406668
• 00887868505256: 406802
• 00887868513084: 406668