Iradimed

GUDID 30889483236370

Iradimed Divided Adult Nasal Canula

SALTER LABS

Nasal oxygen cannula, carbon-dioxide-sampling

• Primary Device ID: 30889483236370
• NIH Device Record Key: 668a0c30-d871-4f58-9d06-79d5c868afc9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Iradimed
• Version Model Number: 1844A
• Company DUNS: 022721133
• Company Name: SALTER LABS
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• 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	10889483295373 [Primary]
GS1	30889483236370 [Package]; Contains: 10889483295373; 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: 2025-08-12
• Device Publish Date: 2025-08-04

On-Brand Devices [Iradimed]

• 30889483236387: Iradimed Divided Pediatric Nasal Canula
• 30889483236370: Iradimed Divided Adult Nasal Canula
• 30889483236363: Iradimed Pediatric Oral / Nasal Cannula
• 30889483236356: Iradimed Adult Oral / Nasal Canula