EM Humeral Resection Guide SSI007558

GUDID 00889024664715

Zimmer, Inc.

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• Primary Device ID: 00889024664715
• NIH Device Record Key: b355c268-9166-4553-a5d6-559a7677062b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EM Humeral Resection Guide
• Version Model Number: SSI007558
• Catalog Number: SSI007558
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024664715 [Primary]

FDA Product Code

• FZX: Guide, Surgical, Instrument

Sterilization

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

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

[00889024664715]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-21
• Device Publish Date: 2024-05-13

On-Brand Devices [EM Humeral Resection Guide]

• 00889024645059: SSI006787
• 00889024664715: SSI007558