AccessGUDID - DEVICE: Medegen Medical Products, LLC (00700812000105)

GUDID

Device Identifier (DI) Information

Brand Name: Medegen Medical Products, LLC
Version or Model: 00081
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: MEDEGEN MEDICAL PRODUCTS, LLC

Primary DI Number: 00700812000105
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 6
Labeler D-U-N-S® Number*: 055527753 *Terms of Use

Device Description: Bedpan Fracture Female Urinal Blue 6/cs

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?
10340	Bedpan, fracture	A device used by a bedridden patient as a receptacle for urine and faeces and which is designed to be used by a patient whose hips have been plastered. This is a reusable device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
FOB	BEDPAN

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 36547300-f75e-408f-99cc-5800a7eb6244
Public Version Date: December 28, 2020
Public Version Number: 1
DI Record Publish Date: December 20, 2020