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BD Leucocount

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Leucocount FDA UDI
Generic Name
White blood cell count IVD, kit, cell count FDA UDI
Device Name
Leucocount Kit w/Trucount Tubes - IVD FDA UDI
Model / Reference
662415 FDA UDI
Description
Leucocount Kit w/Trucount Tubes - IVD FDA UDI

Identifiers

Catalog Number
662415 FDA UDI
Primary DI / UDI-DI
00382906624154 FDA UDI
FDA Product Code
OYE FDA UDI
GKZ FDA UDI
GMDN Term
White blood cell count IVD, kit, cell count 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

No

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

No

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, kit, cell count

BD Leucocount by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as White blood cell count IVD, kit, cell count.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 90429df4-2fad-482a-bcbc-209f2de95573 36 fields · synced May 29, 2026