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CHORUS ADENOVIRUS IgG

FDA UDI

Class I (US FDA UDI)

by Diesse Diagnostica Senese Spa

Identity

Trade Name
CHORUS ADENOVIRUS IgG FDA UDI
Generic Name
Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
81196 FDA UDI

Identifiers

Catalog Number
81196 FDA UDI
Primary DI / UDI-DI
08033891327606 FDA UDI
FDA Product Code
GOD FDA UDI
GMDN Term
Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3020 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

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

CHORUS ADENOVIRUS IgG by Diesse Diagnostica Senese Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Adenovirus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9a5eee62-004a-4dcd-84c7-03d6ac41af00 34 fields · synced May 30, 2026