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Echovirus IgG Control

FDA UDI

Class I (US FDA UDI)

by Bion Enterprises, Ltd.

Identity

Trade Name
Echovirus IgG Control FDA UDI
Generic Name
Multiple enterovirus immunoglobulin G (IgG) antibody IVD, control FDA UDI
Model / Reference
ECG-4420 FDA UDI

Identifiers

Catalog Number
ECG-4420 FDA UDI
Primary DI / UDI-DI
B110ECG44200 FDA UDI
FDA Product Code
GNI FDA UDI
GMDN Term
Multiple enterovirus immunoglobulin G (IgG) antibody IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3205 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Echovirus IgG Control by Bion Enterprises, Ltd. — 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

Sources (1)

  • FDA UDI 51d16ab9-ea12-46d2-af02-09deb14d6419 36 fields · synced Jun 1, 2026