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BD BBL™ Staphyloslide™ Latex Test Kit

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BBL™ Staphyloslide™ Latex Test Kit FDA UDI
Generic Name
Staphylococcus aureus culture isolate antigen IVD, kit, agglutination FDA UDI
Device Name
BD BBL™ Staphyloslide™ Latex Test Kit FDA UDI
Model / Reference
240915 FDA UDI
Description
BD BBL™ Staphyloslide™ Latex Test Kit FDA UDI

Identifiers

Catalog Number
240915 FDA UDI
Primary DI / UDI-DI
00382902409151 FDA UDI
FDA Product Code
GTN FDA UDI
GMDN Term
Staphylococcus aureus culture isolate antigen IVD, kit, agglutination FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3700 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

Dimensions & Sizes

Size
Total Volume — 7.5 Milliliter FDA UDI

Category: Staphylococcus aureus culture isolate antigen IVD, kit, agglutination

BD BBL™ Staphyloslide™ Latex Test Kit by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Staphylococcus aureus culture isolate antigen IVD, kit, agglutination.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI ac9bc3a2-e892-4a2e-a366-67e1f0806861 37 fields · synced May 30, 2026