AccessGUDID - DEVICE: BD BBL™ CDC Anaerobe Laked SB Agar W/Kanamycin and Vancomycin (KV) (10382902218460)

GUDID

Device Identifier (DI) Information

Brand Name: BD BBL™ CDC Anaerobe Laked SB Agar W/Kanamycin and Vancomycin (KV)
Version or Model: 221846
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 221846
Company Name: BECTON, DICKINSON AND COMPANY

Primary DI Number: 10382902218460
Issuing Agency: GS1
Commercial Distribution End Date: September 14, 2022
Device Count: 10
Labeler D-U-N-S® Number*: 122561087 *Terms of Use

Device Description: BD BBL™ CDC Anaerobe Laked Sheep Blood Agar with Kanamycin and Vancomycin (KV)

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
Depth: 15 Millimeter
Outer Diameter: 100 Millimeter

Device Record Status

Public Device Record Key: 723f406a-8186-49c5-8cdb-5cfe48b72b0b
Public Version Date: November 01, 2023
Public Version Number: 2
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
30382902218464	2	10382902218460	2022-09-14	Not in Commercial Distribution	Shelfpack
60382902218465	400	30382902218464	2022-09-14	Not in Commercial Distribution	US pallet