3 Peg Mod Drill Guide Sz 2-5 SSI008203

GUDID 00889024693937

Zimmer, Inc.

Surgical drill guide, reusable

• Primary Device ID: 00889024693937
• NIH Device Record Key: 6ca78ee8-c5de-4e21-95e9-b4681ff63ce9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3 Peg Mod Drill Guide Sz 2-5
• Version Model Number: SSI008203
• Catalog Number: SSI008203
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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

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 Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024693937 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191814

FDA Product Code

• KWT: Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented

Sterilization

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

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

[00889024693937]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-05-01
• Device Publish Date: 2025-04-23

Devices Manufactured by Zimmer, Inc.

• 00889024693937 - 3 Peg Mod Drill Guide Sz 2-5: 2025-05-01
• 00889024693937 - 3 Peg Mod Drill Guide Sz 2-5: 2025-05-01
• 00889024693944 - 3 Peg Mod Drill Guide Sz 1: 2025-05-01
• 00887868139741 - Affixus®: 2025-04-07
• 00887868139758 - Affixus®: 2025-04-07
• 00887868139765 - Affixus®: 2025-04-07
• 00887868139772 - Affixus®: 2025-04-07
• 00887868139789 - Affixus®: 2025-04-07
• 00887868139796 - Affixus®: 2025-04-07