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NOVEOS House Dust - Greer

FDA UDI

Class II (US FDA UDI)

by Hycor Biomedical Llc

Identity

Trade Name
NOVEOS House Dust - Greer FDA UDI
Generic Name
Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent FDA UDI
Model / Reference
H001 FDA UDI

Identifiers

Catalog Number
8633810 FDA UDI
Primary DI / UDI-DI
00816879025026 FDA UDI
FDA Product Code
PUW FDA UDI
GMDN Term
Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5750 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent

NOVEOS House Dust - Greer by Hycor Biomedical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3d3b8d70-b275-4b26-bf46-282d7eb52162 35 fields · synced Jun 6, 2026