acurio

GUDID 16972382160256

XIAMEN ACURIO INSTRUMENT CO.,LTD

Pulse oximeter

• Primary Device ID: 16972382160256
• NIH Device Record Key: 880e69fb-07cf-4c2a-9a25-5ae1a1551ced
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: acurio
• Version Model Number: AS-302
• Company DUNS: 544491528
• Company Name: XIAMEN ACURIO INSTRUMENT 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: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	06972382160266 [Primary]
GS1	16972382160256 [Package]; Contains: 06972382160266; Package: [100 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180685

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: 2022-06-02
• Device Publish Date: 2022-05-25

On-Brand Devices [acurio]

• 16972382160188: AS-302
• 16972382160225: AS-301
• 16972382160256: AS-302