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InstaClear

FDA UDI

Class I (US FDA UDI)

by Aso LLC

Identity

Trade Name
InstaClear FDA UDI
Generic Name
Nasal breathing aid, external FDA UDI
Device Name
Drug-Free Nasal Strips Extra Strength, Clear Strips FDA UDI
Model / Reference
017276233780 FDA UDI
Description
Drug-Free Nasal Strips Extra Strength, Clear Strips FDA UDI

Identifiers

Catalog Number
017276233780 FDA UDI
Primary DI / UDI-DI
00017276233780 FDA UDI
FDA Product Code
LWF FDA UDI
GMDN Term
Nasal breathing aid, external FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.3900 FDA UDI
Commercial Distribution
Not 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

InstaClear by Aso LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aso LLC

Sources (1)

  • FDA UDI c5cc3486-c9cc-4336-9209-70e51284b258 36 fields · synced May 31, 2026