AccessGUDID - DEVICE: Sechrist Industries, Inc. (00852682007064)

GUDID

Device Identifier (DI) Information

Brand Name: Sechrist Industries, Inc.
Version or Model: 21762-111
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: SECHRIST INDUSTRIES, INC.

Primary DI Number: 00852682007064
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2016
Device Count: 1
Labeler D-U-N-S® Number*: 062084215 *Terms of Use

Device Description: WHLD STRCHR, LOW,STD FLT W/BARIATRIC

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):	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?
46148	Patient transfer system, manual	A wheeled stretcher and a mechanism on which a patient can be placed so that the patient can be transferred with minimal disturbance (i.e., without changing horizontal body position, lifting, rolling, or dragging). The device typically includes a patient-transfer mechanism (e.g., mechanical, hydraulic) easy to operate by an attendant with minimal physical effort. It is used in hospitals and other healthcare facilities to reduce injuries to both patients and staff while transferring non-ambulatory, comatose, or neurologically-injured patients between beds, tables, and/or stretchers.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
FPO	Stretcher, Wheeled

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
Width: 53 Inch
Height: 63 Inch
Weight: 300 Pound
Depth: 92 Inch

Device Record Status

Public Device Record Key: 0e58eb02-9818-41f9-a064-71cb38149ae7
Public Version Date: September 27, 2024
Public Version Number: 4
DI Record Publish Date: December 12, 2016