AccessGUDID - DEVICE: MammoPad Radiolucent Cushion (25420045506951)

GUDID

Device Identifier (DI) Information

Brand Name: MammoPad Radiolucent Cushion
Version or Model: MP301-T
Commercial Distribution Status: In Commercial Distribution
Catalog Number: MP301-T
Company Name: Hologic, Inc.

Primary DI Number: 25420045506951
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 10
Labeler D-U-N-S® Number*: 139534114 *Terms of Use

Device Description: The MammoPad® products are designed to provide padding for patient comfort and aid in positioning during radiologic visualization of the breast using x-ray or scintillation technology.

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):	Yes
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?
40899	Radiological breast positioner, non-wearable	A device that is specifically designed to ensure adequate positioning and immobilization of the female patient's breast(s) and chest during diagnostic imaging procedures, image-guided surgical or interventional procedures, and/or radiation therapy procedures. The device is in the form of a frame, board, cushion, or preformed pad (non-wearable device) and may also be used to facilitate reproducible positioning for serial imaging studies or serial radiation therapy treatments.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IZH	System, x-ray, mammographic

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K062141	000

Device Exempt from Premarket Submission: No 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: 96ade932-60b4-4821-9d1b-d02dbc2a8731
Public Version Date: May 22, 2025
Public Version Number: 7
DI Record Publish Date: November 15, 2016