AccessGUDID - DEVICE: PRAS Botulism Selective Medium (BSM) (00810048900176)

GUDID

Device Identifier (DI) Information

Brand Name: PRAS Botulism Selective Medium (BSM)
Version or Model: AS-223
Commercial Distribution Status: In Commercial Distribution
Catalog Number: AS-223
Company Name: ANAEROBE SYSTEMS

Primary DI Number: 00810048900176
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 4
Labeler D-U-N-S® Number*: 021192653 *Terms of Use

Device Description: AS-223 Botulism Selective Medium (BSM) is a selective and differential medium for the presumptive identification of Clostridium botulinum from food or clinical samples. Pre-reduced anaerobically sterilized (PRAS). 100 x 15 mm agar plate. Opaque light yellow. 4 plates per pack.

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):	No
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
JSI	Culture Media, Selective And Differential

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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 20 and 25 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: fd5d5a19-421e-4c81-9383-1f16bb6d9ebd
Public Version Date: May 11, 2020
Public Version Number: 1
DI Record Publish Date: May 01, 2020