Echo® Hip System Instrumentation 31-162396

GUDID 00887868474460

Biomet Orthopedics, LLC

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• Primary Device ID: 00887868474460
• NIH Device Record Key: 5929f9eb-3e3a-4593-8a09-33f9e8f430a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Echo® Hip System Instrumentation
• Version Model Number: 31-162396
• Catalog Number: 31-162396
• 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	00887868474460 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

Moist Heat or Steam Sterilization

[00887868474460]

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 [Echo® Hip System Instrumentation]

• 00887868474590: 31-162415
• 00887868474583: 31-162414
• 00887868474576: 31-162413
• 00887868474569: 31-162406
• 00887868474552: 31-162405
• 00887868474545: 31-162404
• 00887868474538: 31-162403
• 00887868474521: 31-162402
• 00887868474514: 31-162401
• 00887868474507: 31-162400
• 00887868474491: 31-162399
• 00887868474484: 31-162398
• 00887868474477: 31-162397
• 00887868474460: 31-162396
• 00887868474453: 31-162395