AccessGUDID - DEVICE: TrenMAX™ (00696588003856)

GUDID

Device Identifier (DI) Information

Brand Name: TrenMAX™
Version or Model: 415
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 415
Company Name: Innovative Medical Products, Inc

Primary DI Number: 00696588003856
Issuing Agency: GS1
Commercial Distribution End Date: August 24, 2020
Device Count: 5
Labeler D-U-N-S® Number*: 147363154 *Terms of Use

Device Description: TrenMAX™ Pad (5 per case)

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?
62789	Operating table non-slip back pad	A non-slip cushioned pad, typically with a pressure-sensitive adhesive, intended to be placed between an operating table mattress and a patient’s back to secure the patient to the table and prevent them from sliding on the table top, typically while placing them in the Trendelenburg position or applying traction pulling forces on the legs during surgery; it may also be intended to aid in distributing patient body weight over a larger surface area and in preventing pressure sores and tissue necrosis on prominent parts of the body during the procedure. Additional securing devices [e.g., straps, adaptors, clamps] may be included with the device. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FMP	Protector, Skin Pressure

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: be7b81ec-2dfa-4ebc-b7b7-8695a115657b
Public Version Date: July 08, 2021
Public Version Number: 6
DI Record Publish Date: October 14, 2019