← Back to catalogue

BD Difco™ Mueller Hinton Agar

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Difco™ Mueller Hinton Agar FDA UDI
Generic Name
Mueller-Hinton agar antimicrobial susceptibility culture medium IVD FDA UDI
Device Name
BD Difco™ Mueller Hinton Agar FDA UDI
Model / Reference
225230 FDA UDI
Description
BD Difco™ Mueller Hinton Agar FDA UDI

Identifiers

Catalog Number
225230 FDA UDI
Primary DI / UDI-DI
00382902252306 FDA UDI
FDA Product Code
JTZ FDA UDI
GMDN Term
Mueller-Hinton agar antimicrobial susceptibility culture medium IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.1700 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Weight — 10 Kilogram FDA UDI

Category: Mueller-Hinton agar antimicrobial susceptibility culture medium IVD

BD Difco™ Mueller Hinton Agar by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mueller-Hinton agar antimicrobial susceptibility culture medium 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 99d841f1-d520-45ef-af7d-a0d1bd2cd90e 37 fields · synced Jun 8, 2026