eRapid

GUDID 00744229178071

eRapid Nebulizer Handset

PARI RESPIRATORY EQUIPMENT, INC.

Ultrasonic nebulizing system Ultrasonic nebulizing system

• Primary Device ID: 00744229178071
• NIH Device Record Key: 107c1c4a-75b5-48db-9715-f021c9f31dfa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: eRapid
• Version Model Number: 178G8030
• 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: 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	00744229178064 [Primary]
GS1	00744229178071 [Package]; Contains: 00744229178064; Package: carton [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112859

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: 2016-09-26

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• 00744229178071: eRapid Nebulizer Handset
• 00744229178088: eRapid Nebulizer System