Primary Device ID | 00382902252207 |
NIH Device Record Key | e478abff-57d8-4468-8dfc-f6fe4a1bd4f7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Difco™ Mueller Hinton Agar |
Version Model Number | 225220 |
Catalog Number | 225220 |
Company DUNS | 122561087 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)638-8663 |
Technical_services@bd.com | |
Phone | +1(800)638-8663 |
Technical_services@bd.com |
Weight | 2 Kilogram |
Weight | 2 Kilogram |
Storage Environment Temperature | Between 2 Degrees Celsius and 25 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382902252207 [Primary] |
JTZ | CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGAR/BROTH |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00382902252207]
Moist Heat or Steam Sterilization
[00382902252207]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-07-07 |
00382902252504 | BD Difco™ Mueller Hinton Agar |
00382902252306 | BD Difco™ Mueller Hinton Agar |
00382902252207 | BD Difco™ Mueller Hinton Agar |