← Back to catalogue

BD BBL™ Sensi-Disc™ Single Disc Dispenser

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BBL™ Sensi-Disc™ Single Disc Dispenser FDA UDI
Generic Name
Antimicrobial sensitivity disc dispenser IVD FDA UDI
Device Name
BD BBL™ Sensi-Disc™ Single Disc Dispenser FDA UDI
Model / Reference
260459 FDA UDI
Description
BD BBL™ Sensi-Disc™ Single Disc Dispenser FDA UDI

Identifiers

Catalog Number
260459 FDA UDI
Primary DI / UDI-DI
30382902604595 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Antimicrobial sensitivity disc dispenser IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Antimicrobial sensitivity disc dispenser IVD

BD BBL™ Sensi-Disc™ Single Disc Dispenser by Becton Dickinson And Company — Class I — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 93d68c77-e251-42df-88b9-e7c349098102 36 fields · synced May 30, 2026