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IgA RID plate package

FDA UDI

Class I (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
IgA RID plate package FDA UDI
Generic Name
Total immunoglobulin A (IgA total) IVD, antibody FDA UDI
Device Name
Radial immunodiffusion plate package for human IgA FDA UDI
Model / Reference
1 FDA UDI
Description
Radial immunodiffusion plate package for human IgA FDA UDI

Identifiers

Catalog Number
102411 FDA UDI
Primary DI / UDI-DI
B1761024 FDA UDI
FDA Product Code
JZQ FDA UDI
GMDN Term
Total immunoglobulin A (IgA total) IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.4800 FDA UDI
Commercial Distribution
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

No

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: Total immunoglobulin A (IgA total) IVD, antibody

IgA RID plate package by Kent Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total immunoglobulin A (IgA total) IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a5e40e5a-ff30-40f9-9986-861a6fba4555 36 fields · synced Jun 1, 2026