141-01-32

GUDID 10885862026132

LINER DRIVER HEAD, 32mm

Exactech, Inc.

Orthopaedic implant impactor

• Primary Device ID: 10885862026132
• NIH Device Record Key: c7949d7f-dfbd-4d9b-8c58-f9d23758a3dc
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 141-01-32
• Catalog Number: 141-01-32
• Company DUNS: 157565946
• Company Name: Exactech, 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: 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

Device Dimensions

• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 32 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885862026132 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173583

FDA Product Code

• LZO: Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

Sterilization

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

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

[10885862026132]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-02
• Device Publish Date: 2022-08-25

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• 10885862653291 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 4
• 10885862653307 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 5
• 10885862653321 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 1.5
• 10885862653338 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 2.5
• 10885862653345 - Truliant: 2025-01-16 Special Universal Baseplate Tibial Trial, Size 3.5