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Antiserum to Human C-5

FDA UDI

Class II (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
Antiserum to Human C-5 FDA UDI
Generic Name
Complement component C5 IVD, kit, precipitation/immunodiffusion FDA UDI
Device Name
Goat antiserum to Human C-5 FDA UDI
Model / Reference
1 FDA UDI
Description
Goat antiserum to Human C-5 FDA UDI

Identifiers

Catalog Number
110002 FDA UDI
Primary DI / UDI-DI
B176110 FDA UDI
FDA Product Code
DAY FDA UDI
GMDN Term
Complement component C5 IVD, kit, precipitation/immunodiffusion FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5240 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 component C5 IVD, kit, precipitation/immunodiffusion

Antiserum to Human C-5 by Kent Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Complement component C5 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 a558bf23-966f-4cff-948f-cac65d6c0d1f 34 fields · synced May 29, 2026