Bone Marrow Collection Stand X6R2105

GUDID 04086000100380

For use with Bone Marrow Collection Kit

Fresenius Kabi AG

Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole Freestanding/bed-attached intravenous pole

• Primary Device ID: 04086000100380
• NIH Device Record Key: a5f562ba-8024-4223-a2e9-500e46dd3456
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bone Marrow Collection Stand
• Version Model Number: X6R2105
• Catalog Number: X6R2105
• Company DUNS: 315654579
• Company Name: Fresenius Kabi AG
• 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: false
• Serial Number: true
• 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	04086000100380 [Primary]

FDA Product Code

• LWE: Bone Marrow Collection/Transfusion Kit

Sterilization

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

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

[04086000100380]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-08-25
• Device Publish Date: 2022-08-17

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