Nebulizer Compressor Filter

GUDID 10709078005586

Nebulizer Compressor Filter

WESTMED, INC.

Heat/moisture exchanger/microbial filter, non-sterile

• Primary Device ID: 10709078005586
• NIH Device Record Key: bf3187e5-27e3-4dc9-8ff7-2ca6cbcd3237
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nebulizer Compressor Filter
• Version Model Number: 6313
• Company DUNS: 092673953
• Company Name: WESTMED, 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: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00709078005589 [Primary]
GS1	10709078005586 [Package]; Contains: 00709078005589; Package: [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K922492

FDA Product Code

• CAH: Filter, Bacterial, Breathing-Circuit

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: 2019-07-02
• Device Publish Date: 2018-05-16

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