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Ceruloplasmin RID plate package

FDA UDI

Class I (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
Ceruloplasmin RID plate package FDA UDI
Generic Name
Ceruloplasmin IVD, kit, precipitation/immunodiffusion FDA UDI
Device Name
Radial immunodiffusion plate package for Human Ceruloplasmin FDA UDI
Model / Reference
1 FDA UDI
Description
Radial immunodiffusion plate package for Human Ceruloplasmin FDA UDI

Identifiers

Catalog Number
126411 FDA UDI
Primary DI / UDI-DI
B1761264 FDA UDI
FDA Product Code
JZQ FDA UDI
GMDN Term
Ceruloplasmin IVD, kit, precipitation/immunodiffusion 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: Ceruloplasmin IVD, kit, precipitation/immunodiffusion

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

Similar devices

Also classified as Ceruloplasmin IVD, kit, precipitation/immunodiffusion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3d3732d3-c4dd-4b2c-8513-5dae131d70a3 34 fields · synced May 30, 2026