AccessGUDID - DEVICE: RxCrush (00850006611164)

GUDID

Device Identifier (DI) Information

Brand Name: RxCrush
Version or Model: PP10-50
Commercial Distribution Status: In Commercial Distribution
Catalog Number: PP10
Company Name: RESOLVE DESIGNS LLC

Primary DI Number: 00850006611164
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 091290281 *Terms of Use

Device Description: RxCrush Sealed Tear-off Pill Pouch, 2"x5". Sealed pouch for safely holding pills while crushing.

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):	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
KYX	Dispenser, Liquid Medication

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
Special Storage Condition, Specify: Keep out of sunlight. Keep out of moisture.

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f7619d4d-2771-4f24-ab21-10a59b9ff451
Public Version Date: December 25, 2024
Public Version Number: 1
DI Record Publish Date: December 17, 2024

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Status	Package Type
30850006611165	1000	00850006611164	In Commercial Distribution	Box
50850006611169	4000	00850006611164	In Commercial Distribution	Case
10850006611161	5	00850006611164	In Commercial Distribution	SAMPLE