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BD BBL™ DrySlide™ Indole

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BBL™ DrySlide™ Indole FDA UDI
Generic Name
Indole/Kovac's microbial reagent IVD FDA UDI
Device Name
BD BBL™ DrySlide™ Indole FDA UDI
Model / Reference
231748 FDA UDI
Description
BD BBL™ DrySlide™ Indole FDA UDI

Identifiers

Catalog Number
231748 FDA UDI
Primary DI / UDI-DI
30382902317488 FDA UDI
FDA Product Code
JTO FDA UDI
GMDN Term
Indole/Kovac's microbial reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 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

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: Indole/Kovac's microbial reagent IVD

BD BBL™ DrySlide™ Indole by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Indole/Kovac's microbial reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 359dc16c-f735-47ec-b42e-aec537833170 36 fields · synced May 30, 2026