Naväge

FDA UDI

Class II (US FDA UDI)

by Rhinosystems, Inc.

Identity

Trade Name: Naväge FDA UDI
Generic Name: Nasal lavage system FDA UDI
Model / Reference: OSS-1 FDA UDI

Identifiers

Primary DI / UDI-DI: 00858492004545 FDA UDI
FDA Product Code: KDQ FDA UDI
KMA FDA UDI
GMDN Term: Nasal lavage system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6740 FDA UDI
874.5550 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Nasal lavage system

Naväge by Rhinosystems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Rhinosystems, Inc.

Sources (1)

FDA UDI 2412cb65-675b-428e-b4c2-083d4fb3f3fb 33 fields · synced Jun 8, 2026