AccessGUDID - DEVICE: Maxpert Medical MAXCRUSH (00852359007007)

GUDID

Device Identifier (DI) Information

Brand Name: Maxpert Medical MAXCRUSH
Version or Model: E200s
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: MAXPERT MEDICAL

Primary DI Number: 00852359007007
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 066886996 *Terms of Use

Device Description: The MAXCRUSH automatic pill crusher is designed to deliver the maximum amount of crushing effort without the human effort! The MAXCRUSH automatic pill crusher is a portable, battery operated automatic pill crusher system that crushes tablets into a fine powder with the simple push of a button

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:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
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?
15750	Pill crusher/splitter	A hand-held device designed for crushing or splitting in two medication in the form of a tablet for easier ingestion by a patient who cannot swallow the tablet whole. It is designed for convenience to be carried in the user's pocket or handbag (purse) and typically consists of several pieces that can be easily assembled by the user to crush or split the pill (tablet) by screwing the two main body parts against each other. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OHY	Pill Crusher/Cutter

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: e60965c4-8432-4916-ab87-02573c7b6910
Public Version Date: July 23, 2020
Public Version Number: 3
DI Record Publish Date: December 19, 2017