Sample Probe

GUDID 00811403017126

Diamond Diagnostics Inc.

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• Primary Device ID: 00811403017126
• NIH Device Record Key: 14dc9d3e-eba5-4f9a-9915-257b32d7e9b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sample Probe
• Version Model Number: OY-MU9934D
• 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: 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	00811403017126 [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 [Sample Probe]

• 00811403018765: AW-402377D
• 00811403018345: RO-1043864D
• 00811403018307: RO-1029274D
• 00811403010394: AV-BP5006D
• 00811403017126: OY-MU9934D
• 00811403015832: ME-2107D