AccessGUDID - DEVICE: BD BBL™ Campylobacter Agar with 5 Antimicrobics and 10% Sheep Blood (10382902217289)

GUDID

Device Identifier (DI) Information

Brand Name: BD BBL™ Campylobacter Agar with 5 Antimicrobics and 10% Sheep Blood
Version or Model: 221728
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 221728
Company Name: BECTON, DICKINSON AND COMPANY

Primary DI Number: 10382902217289
Issuing Agency: GS1
Commercial Distribution End Date: March 14, 2022
Device Count: 10
Labeler D-U-N-S® Number*: 122561087 *Terms of Use

Device Description: BD BBL™ Campylobacter Agar with 5 Antimicrobics and 10% Sheep Blood

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
58585	Differential/selective agar culture medium IVD	An agar culture medium intended to be used to promote the selective growth of a microbial species with specific characteristics (e.g., antibiotic resistance, ability to utilize, synthesize specific metabolites) and/or distinguish between microbial species growing on the same medium by appearance (e.g., colour, shape, growth pattern). It typically contains substances to inhibit the growth of commensal or contaminating microorganisms (e.g., antimicrobials, dyes, salts) and/or dyes or chemical indicators for differentiation.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JSJ	CULTURE MEDIA, SELECTIVE AND NON-DIFFERENTIAL

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 100 Millimeter
Depth: 15 Millimeter

Device Record Status

Public Device Record Key: 5021ed87-ecda-4ec1-a806-b202637ed281
Public Version Date: October 28, 2024
Public Version Number: 3
DI Record Publish Date: May 25, 2018

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
30382902217283	10	10382902217289	2022-03-14	Not in Commercial Distribution	Shelfpack
60382902217284	96	30382902217283	2022-03-14	Not in Commercial Distribution	US pallet