Mindray Cannula 4700

GUDID 30889483555013

Mindray Infant EtCO2-O2 Nasal Divided Cannula

SALTER LABS

Nasal oxygen cannula, carbon-dioxide-sampling

• Primary Device ID: 30889483555013
• NIH Device Record Key: f67933ca-2a45-464d-86be-67ce3a7390d1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mindray Cannula
• Version Model Number: SO-2178
• Catalog Number: 4700
• Company DUNS: 022721133
• Company Name: SALTER LABS
• 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10889483555026 [Primary]
GS1	30889483555013 [Package]; Contains: 10889483555026; Package: [25 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151421

FDA Product Code

• CCK: Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

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: 2024-07-15
• Device Publish Date: 2024-07-05

On-Brand Devices [Mindray Cannula]

• 30889483555068: Mindray Pediatric EtCO2-O2 Nasal Divided Cannula
• 30889483555044: Mindray Adult EtCO2-O2 Nasal Divided Cannula
• 30889483555013: Mindray Infant EtCO2-O2 Nasal Divided Cannula