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BD BBL™ Prompt™ Inoculation System

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BBL™ Prompt™ Inoculation System FDA UDI
Generic Name
Antimicrobial sensitivity disc dispenser IVD FDA UDI
Device Name
BD BBL™ Prompt™ Inoculation System FDA UDI
Model / Reference
226306 FDA UDI
Description
BD BBL™ Prompt™ Inoculation System FDA UDI

Identifiers

Catalog Number
226306 FDA UDI
Primary DI / UDI-DI
30382902263068 FDA UDI
510(k) Number
K820299 FDA UDI
FDA Product Code
LIE FDA UDI
GMDN Term
Antimicrobial sensitivity disc dispenser IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.1640 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

No

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: Antimicrobial sensitivity disc dispenser IVD

BD BBL™ Prompt™ Inoculation System by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antimicrobial sensitivity disc dispenser IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f46e80a8-2e19-4eed-887f-904482861491 37 fields · synced May 30, 2026