Custom Pack

GUDID 10848340002400

Custom Pack

ADVANCE MEDICAL DESIGNS, INC.

Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use

• Primary Device ID: 10848340002400
• NIH Device Record Key: 946a41ce-860d-499a-bb08-00dca163be6a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Custom Pack
• Version Model Number: 08-PK106
• Company DUNS: 130785884
• Company Name: ADVANCE MEDICAL DESIGNS, INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• 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	00848340002403 [Primary]
GS1	10848340002400 [Package]; Contains: 00848340002403; Package: [25 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K850959

FDA Product Code

• JAA: System, x-ray, fluoroscopic, image-intensified

Sterilization

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

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

[10848340002400]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-29
• Device Publish Date: 2024-02-21

On-Brand Devices [Custom Pack]

• 10848340002325: Disposable Equipment Cover
• 10848340002332: Disposable Equipment Cover
• 10848340002417: Custom Pack
• 10848340002400: Custom Pack