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Antithrombin III RID plate package

FDA UDI

Class II (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
Antithrombin III RID plate package FDA UDI
Generic Name
Antithrombin III (ATIII) IVD, kit, precipitation/immunodiffusion FDA UDI
Device Name
Radial immunodiffusion plate package for Human Antithrombin III with standards FDA UDI
Model / Reference
1 FDA UDI
Description
Radial immunodiffusion plate package for Human Antithrombin III with standards FDA UDI

Identifiers

Catalog Number
148511 FDA UDI
Primary DI / UDI-DI
B1761485 FDA UDI
FDA Product Code
JBQ FDA UDI
GMDN Term
Antithrombin III (ATIII) IVD, kit, precipitation/immunodiffusion FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.7060 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: Antithrombin III (ATIII) IVD, kit, precipitation/immunodiffusion

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

Similar devices

Also classified as Antithrombin III (ATIII) IVD, kit, precipitation/immunodiffusion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kent Laboratories, Inc.

Sources (1)

  • FDA UDI d752a5a6-202e-4041-a78f-b73aca811db4 34 fields · synced May 30, 2026