TROCAR SCREW PIN DRIVER SSI007585

GUDID 00889024670778

Zimmer, Inc.

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• Primary Device ID: 00889024670778
• NIH Device Record Key: f8ea4992-ca1f-4122-a165-0517f61c0c4b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TROCAR SCREW PIN DRIVER
• Version Model Number: SSI007585
• Catalog Number: SSI007585
• 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	00889024670778 [Primary]

FDA Product Code

• HWB: Extractor

Sterilization

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

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

Moist Heat or Steam Sterilization

[00889024670778]

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

Devices Manufactured by Zimmer, Inc.

• 00889024673434 - RIGID SUPRA ENTRY SLEEVE 13MM: 2024-06-14
• 00889024673441 - RIGID SUPRA ENTRY SLEEVE 15MM: 2024-06-14
• 00889024673458 - RIGID SUPRA ENTRY SLEEVE TIBIAL PIN FIX 13MM: 2024-06-14
• 00889024673465 - RIGID SUPRA ENTRY SLEEVE TIBIAL PIN FIX 15MM: 2024-06-14
• 00889024673779 - ALLIANCE UNIV AUG SIZER SZ 2: 2024-06-14
• 00889024673786 - ALLIANCE UNIV AUG SIZER SZ 3: 2024-06-14
• 00889024673793 - ALLIANCE UNIV AUG SIZER SZ 4: 2024-06-14
• 00889024673809 - ALLIANCE UNIV AUG SIZER SZ 5: 2024-06-14