Foot plate

GUDID 04046768001480

MAQUET GmbH

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• Primary Device ID: 04046768001480
• NIH Device Record Key: 6b920941-93d8-4a42-80d8-2ae26bdc0e3e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Foot plate
• Version Model Number: 100197A0
• Company DUNS: 315435859
• Company Name: MAQUET GmbH
• 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: true
• Manufacturing Date: true
• 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	04046768001480 [Primary]

FDA Product Code

• BWN: TABLE AND ATTACHMENTS, OPERATING-ROOM

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-30
• Device Publish Date: 2022-09-22

On-Brand Devices [Foot plate]

• 04046768038691: 100197Y0
• 04046768001480: 100197A0
• 04046768000049: 10018700