JULIET Ti PO JUL-BX 40 11-N

GUDID 07640332471012

JULIET COMBO SET - TRIALS RACK PO NARROW

SpineArt SA

Instrument tray, reusable

• Primary Device ID: 07640332471012
• NIH Device Record Key: 8ffcd0cb-600a-4fe3-954a-c93fdcaa2362
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JULIET Ti PO
• Version Model Number: JUL-BX 40 11-N
• Catalog Number: JUL-BX 40 11-N
• Company DUNS: 483016148
• Company Name: SpineArt SA
• 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: true
• Serial Number: false
• Manufacturing Date: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	07640332471012 [Primary]

FDA Product Code

• FSM: Tray, Surgical, Instrument

Sterilization

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

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

[07640332471012]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-11-28
• Device Publish Date: 2025-11-20

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