Pump Tubing

GUDID 00811403013630

Diamond Diagnostics Inc.

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• Primary Device ID: 00811403013630
• NIH Device Record Key: 55a5bb06-8da6-45de-93cb-9d61ccb56cc5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pump Tubing
• Version Model Number: CD-673705D
• Company DUNS: 947514303
• Company Name: Diamond Diagnostics Inc.
• 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: true
• Device Combination Product: false
• Single Use: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811403013630 [Primary]

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: 2023-06-21
• Device Publish Date: 2023-06-13

On-Brand Devices [Pump Tubing]

• 00811403018819: AW-906182D
• 00811403017164: RD-842194D
• 00811403015818: ME-2104D
• 00811403013630: CD-673705D