SenTec Digital Monitor (with activated PO2 channel

GUDID 07640121880759

Stand alone monitor with colour display for continuous non-invasive vital parameter monitoring, with integrated docking station for sensor storage and

SenTec AG

Transcutaneous blood gas monitoring system

• Primary Device ID: 07640121880759
• NIH Device Record Key: bb2184e3-1e78-423a-b5d3-564d7ff90540
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SenTec Digital Monitor (with activated PO2 channel
• Version Model Number: SDM-PO2
• Company DUNS: 480797856
• Company Name: SenTec AG
• 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: false
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C
• Special Storage Condition, Specify: Between 0 and 0 *during transport: 0-50°C

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640121880759 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041548

FDA Product Code

• DPZ: Oximeter, Ear

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-31

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• EIT11ST2721000 - 1ST272-100 LuMon™ Belt Size 19: 2025-09-16
• EIT11ST2731000 - 1ST273-100 LuMon™ Belt Size 22: 2025-09-16
• EIT11ST2741000 - 1ST274-100 LuMon™ Belt Size 26: 2025-09-16
• EIT11ST2751000 - 1ST275-100 LuMon™ Belt Size 30: 2025-09-16
• EIT11ST2761000 - 1ST276-100 LuMon™ Belt Size 35: 2025-09-16
• EIT11ST2771000 - 1ST277-100 LuMon™ Belt Size 40: 2025-09-16