PIVOTING HUMERAL EM GUIDE SSI007211

GUDID 00889024658004

Zimmer, Inc.

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• Primary Device ID: 00889024658004
• NIH Device Record Key: 8894d590-dcec-42af-94c5-15e1f3e3c86d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PIVOTING HUMERAL EM GUIDE
• Version Model Number: SSI007211
• Catalog Number: SSI007211
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• 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: false
• Serial Number: true
• 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) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com
• Phone: 1 (800) 343-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024658004 [Primary]

FDA Product Code

• FZX: Guide, Surgical, Instrument

Sterilization

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

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

[00889024658004]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-25
• Device Publish Date: 2023-12-15

Devices Manufactured by Zimmer, Inc.

• 00889024660595 - BIOMET Anterior Adapter: 2024-04-23
• 00889024660601 - BIOMET Posterior Adapter: 2024-04-23
• 00889024660816 - +9MM Spacer Block C/D 10mm: 2024-04-23
• 00889024660823 - +9MM Spacer Block C/D 12mm: 2024-04-23
• 00889024660830 - +9MM Spacer Block C/D 14mm: 2024-04-23
• 00889024660847 - +9MM Spacer Block C/D 16mm: 2024-04-23
• 00889024660854 - +9MM Spacer Block C/D 18mm: 2024-04-23
• 00889024660861 - +9MM Spacer Block C/D 20mm: 2024-04-23