Viatom

GUDID 06934440100010

Shenzhen Viatom Technology Co., Ltd.

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• Primary Device ID: 06934440100010
• NIH Device Record Key: e009c1e5-f24d-4d9b-a307-e701e4801bea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Viatom
• Version Model Number: Checkme Pro Health Monitor
• Company DUNS: 421357243
• Company Name: Shenzhen Viatom Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06934440100010 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150869

FDA Product Code

• MWI: Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

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: 2020-09-09
• Device Publish Date: 2019-07-23

On-Brand Devices [Viatom]

• 06934440100010: Checkme Pro Health Monitor
• 06934440100676: Oxiband (Checkme) O2 Pulse Oximeter
• 06934440101994: PO6 Oxyfit Pulse Oximeter
• 16934440100024: PO6 Oxyfit Pulse Oximeter