Lamira

GUDID 00744229100683

Lamira Nebulizer Aerosol Head

PARI RESPIRATORY EQUIPMENT, INC.

Ultrasonic nebulizing system

• Primary Device ID: 00744229100683
• NIH Device Record Key: cce08f6e-66e8-4282-8ed3-394388a150a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lamira
• Version Model Number: 078F2671
• Company DUNS: 804736098
• Company Name: PARI RESPIRATORY EQUIPMENT, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00744229100683 [Package]; Contains: 00744229789116; Package: carton [160 Units]; In Commercial Distribution
GS1	00744229789116 [Primary]

FDA Product Code

• CAF: Nebulizer (Direct Patient Interface)

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: 2019-02-08
• Device Publish Date: 2019-01-08

On-Brand Devices [Lamira]

• 00744229100683: Lamira Nebulizer Aerosol Head
• 00744229100669: Lamira Nebulizer Handset
• 00744229100676: Lamira Nebulizer System