← Back to catalogue

Anti Human Properdin FITC

FDA UDI

Class I (US FDA UDI)

by Kent Laboratories, Inc.

Identity

Trade Name
Anti Human Properdin FITC FDA UDI
Generic Name
Complement reagent IVD FDA UDI
Device Name
Fluorescein conjugated polyclonal goat antiserum to Human Complement Properdin FDA UDI
Model / Reference
1 FDA UDI
Description
Fluorescein conjugated polyclonal goat antiserum to Human Complement Properdin FDA UDI

Identifiers

Catalog Number
108202 FDA UDI
Primary DI / UDI-DI
B1761082 FDA UDI
FDA Product Code
DHL FDA UDI
GMDN Term
Complement reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.4100 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 reagent IVD

Anti Human Properdin FITC by Kent Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Complement reagent IVD.

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 497f95f3-e481-4776-8613-6812497b40d9 36 fields · synced Jun 1, 2026