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BD BBL™ MGIT™ PANTA™ Antibiotic Mixture

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD BBL™ MGIT™ PANTA™ Antibiotic Mixture FDA UDI
Generic Name
Culture medium antimicrobial supplement IVD FDA UDI
Device Name
BD BBL™ MGIT™ PANTA™ Antibiotic Mixture, lyophilized, carton of 6 vials. Each vial sufficient for 25 MGIT tubes FDA UDI
Model / Reference
245114 FDA UDI
Description
BD BBL™ MGIT™ PANTA™ Antibiotic Mixture, lyophilized, carton of 6 vials. Each vial sufficient for 25 MGIT tubes FDA UDI

Identifiers

Catalog Number
245114 FDA UDI
Primary DI / UDI-DI
30382902451144 FDA UDI
FDA Product Code
MDB FDA UDI
GMDN Term
Culture medium antimicrobial supplement IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2560 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

Yes

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: Culture medium antimicrobial supplement IVD

BD BBL™ MGIT™ PANTA™ Antibiotic Mixture by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Culture medium antimicrobial supplement IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b6eeaf5e-ecdd-410f-9425-b0e9d6bf07dc 36 fields · synced May 30, 2026