TeleRPM

GUDID 00850042929445

Mio Labs Inc.

Pulse oximeter

• Primary Device ID: 00850042929445
• NIH Device Record Key: 8299b771-47bd-48e9-a6a6-13d07276d0e1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TeleRPM
• Version Model Number: TRK01
• Company DUNS: 117119317
• Company Name: Mio Labs 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• 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	00850042929445 [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: 2024-04-10
• Device Publish Date: 2024-04-02

On-Brand Devices [TeleRPM]

• 00850042929452: YM402
• 00850042929445: TRK01