LC Sprint

GUDID 00744229100249

LC Sprint Nebulizer Kit, Vios Pro

PARI RESPIRATORY EQUIPMENT, INC.

Nebulizing system delivery set, reusable

• Primary Device ID: 00744229100249
• NIH Device Record Key: b943541a-5bf8-4ab2-9d60-8f97c5833c14
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LC Sprint
• Version Model Number: 023F35-VP
• Company DUNS: 804736098
• Company Name: PARI RESPIRATORY EQUIPMENT, 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00744229100249 [Package]; Contains: 00744229230151; Package: carton [50 Units]; In Commercial Distribution
GS1	00744229230151 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K060399

FDA Product Code

• CAF: Nebulizer (Direct Patient Interface)

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: 2018-07-06
• Device Publish Date: 2016-09-30

On-Brand Devices [LC Sprint]

• 00744229100263: LC Sprint Junior Nebulizer Kit, Vios Pro
• 00744229100249: LC Sprint Nebulizer Kit, Vios Pro
• 00744229100232: LC Sprint Nebulizer Kit Retail
• 00744229100225: LC Sprint Neb Set
• 00744229100737: PARI LC Sprint, Nebulizer Set, PRO