AccessGUDID - DEVICE: Medegen Medical Products, LLC (00700812007401)

GUDID

Device Identifier (DI) Information

Brand Name: Medegen Medical Products, LLC
Version or Model: P02-B1202-10
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: MEDEGEN MEDICAL PRODUCTS, LLC

Primary DI Number: 00700812007401
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 300
Labeler D-U-N-S® Number*: 055527753 *Terms of Use

Device Description: Container 120ml St 300/cs 20/plt

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":	Yes
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?
31400	Sterile urine specimen container IVD	A sterile covered plastic receptacle with no additives intended to be used for the collection, and preservation and/or transport, of a urine specimen for culture, analysis, and/or other investigation. This is a single-use device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
FMH	CONTAINER, SPECIMEN, STERILE

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: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 758c3f48-fbde-4ea9-a492-c43b0a9dc5e2
Public Version Date: December 28, 2020
Public Version Number: 1
DI Record Publish Date: December 20, 2020