Flexible Shaft Entry Reamer 211201103

GUDID 00887868561351

Biomet Orthopedics, LLC

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• Primary Device ID: 00887868561351
• NIH Device Record Key: 8602d585-c084-449d-b8bc-ace629afaa3d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flexible Shaft Entry Reamer
• Version Model Number: 2112-01-103
• Catalog Number: 211201103
• 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
• 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	00887868561351 [Primary]

FDA Product Code

• HTO: REAMER

Sterilization

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

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

[00887868561351]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-15
• Device Publish Date: 2023-09-07

Devices Manufactured by Biomet Orthopedics, LLC

• 00887868004087 - PRIMARY TREPHINE: 2024-04-03
• 00887868004094 - BUSHING: 2024-04-03
• 00887868004100 - SECONDARY TREPHINE: 2024-04-03
• 00887868048272 - TREPHINE: 2024-04-03
• 00887868048289 - TREPHINE: 2024-04-03
• 00887868048296 - TREPHINE: 2024-04-03
• 00887868048302 - TREPHINE: 2024-04-03
• 00880304658387 - Compress®: 2024-03-11