Type I Taper Modular Head 31-482596

GUDID 00887868481840

Biomet Orthopedics, LLC

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• Primary Device ID: 00887868481840
• NIH Device Record Key: 7df73144-d0a5-490a-8ad1-5ac921817c30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Type I Taper Modular Head
• Version Model Number: 31-482596
• Catalog Number: 31-482596
• 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	00887868481840 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

Moist Heat or Steam Sterilization

[00887868481840]

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 [Type I Taper Modular Head]

• 00887868481840: 31-482596
• 00887868481833: 31-482595
• 00887868481826: 31-482594
• 00887868481819: 31-482593
• 00887868481802: 31-482592
• 00887868481796: 31-482591
• 00887868481789: 31-482590