RingLoc®+ Max-Rom™ 33-115822

GUDID 00887868501982

Biomet Orthopedics, LLC

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• Primary Device ID: 00887868501982
• NIH Device Record Key: db48d360-fa1a-4a01-9438-daf35e5e9990
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RingLoc®+ Max-Rom™
• Version Model Number: 33-115822
• Catalog Number: 33-115822
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00887868501982 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

[00887868501982]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-16
• Device Publish Date: 2022-05-08

On-Brand Devices [RingLoc®+ Max-Rom™]

• 00887868501982: 33-115822
• 00887868502040: 33-115828
• 00887868502033: 33-115827
• 00887868502026: 33-115826
• 00887868502019: 33-115825
• 00887868502002: 33-115824
• 00887868501999: 33-115823
• 00887868501975: 33-115821