181-00-06

GUDID 10885862241535

DRILL GUIDE, 3.2mm

Exactech, Inc.

Surgical guillotine

• Primary Device ID: 10885862241535
• NIH Device Record Key: 3700f358-f1a3-4524-a899-b1617265989b
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 181-00-06
• Catalog Number: 181-00-06
• 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

• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 3.2 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885862241535 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K141797

FDA Product Code

• JWH: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

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

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

[10885862241535]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-12
• Device Publish Date: 2022-10-04

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