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C-3 Proactivator RID plate kit

FDA UDI

Class I (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
C-3 Proactivator RID plate kit FDA UDI
Generic Name
Complement factor B IVD, kit precipitation/immunodiffusion FDA UDI
Device Name
Radial immunodiffusion plate package for Human C-3 Proactivator with standards FDA UDI
Model / Reference
1 FDA UDI
Description
Radial immunodiffusion plate package for Human C-3 Proactivator with standards FDA UDI

Identifiers

Catalog Number
106511 FDA UDI
Primary DI / UDI-DI
B1761065 FDA UDI
FDA Product Code
JZQ FDA UDI
GMDN Term
Complement factor B 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: Complement factor B IVD, kit precipitation/immunodiffusion

C-3 Proactivator RID plate kit by Kent Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Complement factor B 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 d1185945-815b-4c89-92c6-b94031da3191 34 fields · synced May 30, 2026