AccessGUDID - DEVICE: Strideway MR Tile (B970MRSW40)

GUDID

Device Identifier (DI) Information

Brand Name: Strideway MR Tile
Version or Model: 4-Tile Medium Resolution Strideway System
Commercial Distribution Status: In Commercial Distribution
Catalog Number: MRSW4
Company Name: Tekscan, Inc.

Primary DI Number: B970MRSW40
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 178180246 *Terms of Use

Device Description: Includes 4 Medium Resolution Strideway Tiles, 1 pair of End Caps, 1 Rollout Cover, 1 Strideway Power Supply, 1 AC Power Cord for North America, 1 Strideway USB Data Cable, Strideway Software, Equilibration Files, 3162 Sensor Map, Strideway Shipping Case, PDF of the Users Manual, Printed Copy of the Quick Start Note, and 1 Training Session (USA Only)

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):	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?
43829	Body-surface pressure mapping system	An assembly of electronic devices intended to be used to measure the contact pressure between the body surface and a pressure-sensing pad to provide a map of compression forces during planning of/preparation for personal mobility device use or body support device use by a patient. Described as pressure mapping technology (PMT), it includes a sensor pad and a dedicated computer/software for data analysis, and is typically used to customize the shape of a wheelchair seating cushion to reduce the risk of pressure sore development.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JFC	System, Pressure Measurement, Intermittent

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: 3bf30137-6cd7-4ec1-b2b2-e6a3cac5e8b5
Public Version Date: November 19, 2020
Public Version Number: 2
DI Record Publish Date: November 03, 2020