← Back to catalogue

Alpha 2 Macroglobulin RID kit

FDA UDI

Class I (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
Alpha 2 Macroglobulin RID kit FDA UDI
Generic Name
Alpha-2-macroglobulin IVD, reagent FDA UDI
Device Name
Radial immunodiffusion plate package for Human Alpha 2 Macroglobulin with standards FDA UDI
Model / Reference
1 FDA UDI
Description
Radial immunodiffusion plate package for Human Alpha 2 Macroglobulin with standards FDA UDI

Identifiers

Catalog Number
124511 FDA UDI
Primary DI / UDI-DI
B1761245 FDA UDI
FDA Product Code
JZQ FDA UDI
GMDN Term
Alpha-2-macroglobulin IVD, reagent 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: Alpha-2-macroglobulin IVD, reagent

Alpha 2 Macroglobulin RID kit by Kent Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alpha-2-macroglobulin IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Kent Laboratories, Inc.

Sources (1)

  • FDA UDI 63b37f3d-1047-4296-a9d3-98f3987041a2 34 fields · synced May 30, 2026