NuvoMed

GUDID 00810110303676

TFT Pulse Oximeter

NUVOMED, INC.

Pulse oximeter

• Primary Device ID: 00810110303676
• NIH Device Record Key: 719141bd-9c00-4d38-b012-c726d363add1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NuvoMed
• Version Model Number: LOS-12/0367
• Company DUNS: 080809709
• Company Name: NUVOMED, 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	00810110303676 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240092

FDA Product Code

• DQA: Oximeter

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: 2024-12-23
• Device Publish Date: 2024-12-13

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