Lifecard CFC256MB

GUDID 10841522131103

256 MB COMPACT FLASH CARD

SPACELABS HEALTHCARE (WASHINGTON), INC

Electrocardiographic ambulatory recorder

• Primary Device ID: 10841522131103
• NIH Device Record Key: 4821ed29-5e5f-44c7-9b3d-ae5733396f3d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lifecard
• Version Model Number: Compact Flash Card
• Catalog Number: CFC256MB
• Company DUNS: 145581588
• Company Name: SPACELABS HEALTHCARE (WASHINGTON), 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: 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	10841522131103 [Primary]

FDA Product Code

• MWJ: Electrocardiograph, ambulatory (without analysis)

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: 2023-08-29
• Device Publish Date: 2023-08-21

On-Brand Devices [Lifecard]

• 10841522131103: 256 MB COMPACT FLASH CARD
• 10841522131097: 90 MB COMPACT FLASH CARD