500mm Carbon Fiber Rod

GUDID 00810028396371

Medshape, Inc.

Orthopaedic fixation plate, non-bioabsorbable

• Primary Device ID: 00810028396371
• NIH Device Record Key: 32056244-695e-420a-ab24-6f95f916659e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 500mm Carbon Fiber Rod
• Version Model Number: DNE-9000-500-CF
• Company DUNS: 601306413
• Company Name: Medshape, 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810028396371 [Primary]

FDA Product Code

• KTT: Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Sterilization

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

[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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[00810028396371]

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Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-07-09
• Device Publish Date: 2024-05-31

On-Brand Devices [500mm Carbon Fiber Rod]

• 00810028397132: DNE-9000-500-CF
• 00810028396371: DNE-9000-500-CF