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Alzair

FDA UDI

Class II (US FDA UDI)

by Hudson Scientific Llc

Identity

Trade Name
Alzair FDA UDI
Generic Name
Nasal air filter, topical FDA UDI
Device Name
Alzair is a natural powder product that works by strengthening one's resistance to allergens via a nasal spray with a patented delivery system. FDA UDI
Model / Reference
Allergy Blocker FDA UDI
Description
Alzair is a natural powder product that works by strengthening one's resistance to allergens via a nasal spray with a patented delivery system. FDA UDI

Identifiers

Catalog Number
50131 FDA UDI
Primary DI / UDI-DI
00370914030012 FDA UDI
510(k) Number
K170848 FDA UDI
FDA Product Code
NUP FDA UDI
GMDN Term
Nasal air filter, topical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5045 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 800 Milligram FDA UDI

Alzair by Hudson Scientific Llc — Class II — 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

Sources (1)

  • FDA UDI 03195c53-1fa0-456c-a47c-ea0b6572db63 39 fields · synced May 30, 2026