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NeilMed Nasogel

FDA UDI

Class I (US FDA UDI)

by NeilMed Pharmaceuticals Inc.

Identity

Trade Name
NeilMed Nasogel FDA UDI
Generic Name
Nasal mucosa dressing, non-antimicrobial FDA UDI
Device Name
Nasogel provides moisture to hydrate and lubricate dry and nasal passages caused by dry climate and indoor heat. It helps reduce nasal dryness experienced during air travel, oxygen, sleep apnea equipment device as well as dryness symptoms caused by various medical conditions. FDA UDI
Model / Reference
Nasogel Spray FDA UDI
Description
Nasogel provides moisture to hydrate and lubricate dry and nasal passages caused by dry climate and indoor heat. It helps reduce nasal dryness experienced during air travel, oxygen, sleep apnea equipment device as well as dryness symptoms caused by various medical conditions. FDA UDI

Identifiers

Catalog Number
GSP30-6R-96-ENU-USL FDA UDI
Primary DI / UDI-DI
00705928045309 FDA UDI
FDA Product Code
KCJ FDA UDI
GMDN Term
Nasal mucosa dressing, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5220 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasal mucosa dressing, non-antimicrobial

NeilMed Nasogel by NeilMed Pharmaceuticals Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal mucosa dressing, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f787b90c-189e-4205-ae3f-4876a2adb6b8 34 fields · synced May 30, 2026