PULMO-PROTECT BREATHING FILTER WITH FLEXIBLE MOUTHPIECE AND NOSE CLIP

GUDID 05030267146505

PULMO-PROTECT BREATHING FILTER WITH FLEXIBLE MOUTHPIECE AND NOSE CLIP

Intersurgical Incorporated

Pulmonary function testing kit Pulmonary function testing kit Pulmonary function testing kit Pulmonary function testing kit Pulmonary function testing kit Pulmonary function testing kit Pulmonary function testing kit Pulmonary function testing kit Pulmonary function testing kit

• Primary Device ID: 05030267146505
• NIH Device Record Key: a95ea9de-941a-41c8-8853-076bf9bd1aa3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PULMO-PROTECT BREATHING FILTER WITH FLEXIBLE MOUTHPIECE AND NOSE CLIP
• Version Model Number: 1691013
• Company DUNS: 785952607
• Company Name: Intersurgical Incorporated
• 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: true
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 3154512900
• Email: support@intersurgicalinc.com
• Phone: 3154512900
• Email: support@intersurgicalinc.com
• Phone: 3154512900
• Email: support@intersurgicalinc.com
• Phone: 3154512900
• Email: support@intersurgicalinc.com
• Phone: 3154512900
• Email: support@intersurgicalinc.com
• Phone: 3154512900
• Email: support@intersurgicalinc.com
• Phone: 3154512900
• Email: support@intersurgicalinc.com
• Phone: 3154512900
• Email: support@intersurgicalinc.com
• Phone: 3154512900
• Email: support@intersurgicalinc.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05030267146499 [Primary]
GS1	05030267146505 [Package]; Contains: 05030267146499; Package: [30 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K013123

FDA Product Code

• BZG: Spirometer, Diagnostic

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: 2022-07-25
• Device Publish Date: 2022-07-15

On-Brand Devices [PULMO-PROTECT BREATHING FILTER WITH FLEXIBLE MOUTHPIECE AND NOSE CLIP]

• 05030267146505: PULMO-PROTECT BREATHING FILTER WITH FLEXIBLE MOUTHPIECE AND NOSE CLIP
• 05030267146444: PULMO-PROTECT BREATHING FILTER WITH FLEXIBLE MOUTHPIECE AND NOSE CLIP