← Back to catalogue

Whole Blood Lysing Reagent

FDA UDI

Class II (US FDA UDI)

by Beckman Coulter, Inc.

Identity

Trade Name
Whole Blood Lysing Reagent FDA UDI
Generic Name
White blood cell count IVD, reagent FDA UDI
Device Name
Whole Blood Lysing Reagents FDA UDI
Model / Reference
300 tests FDA UDI
Description
Whole Blood Lysing Reagents FDA UDI

Identifiers

Catalog Number
6603152 FDA UDI
Primary DI / UDI-DI
15099590543389 FDA UDI
FDA Product Code
GKZ FDA UDI
GMDN Term
White blood cell count IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5220 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: White blood cell count IVD, reagent

Whole Blood Lysing Reagent by Beckman Coulter, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as White blood cell count IVD, reagent.

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

Sources (1)

  • FDA UDI 781b4878-e859-469c-b357-e5ffad4ea001 35 fields · synced Jun 8, 2026