Innomed, Inc. 1112

GUDID 00840277100054

Lombardi Tibia Cement Preparation Drill Bit

INNOMED, INC.

Surgical drill guide, reusable

• Primary Device ID: 00840277100054
• NIH Device Record Key: bb3ef48b-62ab-4d3c-a195-b7f39de2600b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Innomed, Inc.
• Version Model Number: 1112
• Catalog Number: 1112
• Company DUNS: 878427491
• Company Name: INNOMED, 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: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840277100054 [Primary]

FDA Product Code

• FZX: Guide, Surgical, Instrument

Sterilization

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

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

[00840277100054]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-26
• Device Publish Date: 2020-05-18

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