Naväge

GUDID 00858492004002

Rhinosystems, Inc.

Nasal lavage system

• Primary Device ID: 00858492004002
• NIH Device Record Key: 1c26047d-4a7c-426e-ac87-db781de0ddd9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Naväge
• Version Model Number: SGD2
• Company DUNS: 008016231
• Company Name: Rhinosystems, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 1-800-203-6400
• Email: support@navage.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00858492004002 [Primary]

FDA Product Code

• KDQ: Bottle, Collection, Vacuum

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-28
• Device Publish Date: 2016-09-21

On-Brand Devices [Naväge ]

• 00858492004545: OSS-1
• 00858492004002: SGD2
• 00858492004644: EUC-1
• 00858492004224: SDG-2 OSS-1
• 00858492004958: ALK-1