AccessGUDID - DEVICE: LiftMate (00728564000006)

GUDID

Device Identifier (DI) Information

Brand Name: LiftMate
Version or Model: 3000
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 3000
Company Name: The Brewer Company LLC

Primary DI Number: 00728564000006
Issuing Agency: GS1
Commercial Distribution End Date: October 17, 2018
Device Count: 1
Labeler D-U-N-S® Number*: 006073399 *Terms of Use

Device Description: The Brewer LiftMate Patient Lift is used in examination rooms for safely lifting patients with mobility issues onto exam tables.

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):	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?
30021	Freestanding patient lifting system, electrically-powered	An electrically-powered, stationary (non-mobile) assembly of devices designed to enable one person to lift and move an incapacitated patient or a person with a disability safely and with minimal physical effort within an area limited by the lifting radius of the system. Also known as a patient hoist, it typically consists of a support base (non-fixed and freestanding on the floor) with a motorized lifting mechanism, mast, boom/lifting arm(s), swivel bar, and patient holding device (e.g., a sling, holder or a frame). Repositioning of the assembly may be achieved by lifting it to a new position/location.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FNG	Lift, Patient, Ac-Powered

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: 7b88deef-cc34-4e3a-9a92-570b1bc42f04
Public Version Date: December 13, 2022
Public Version Number: 4
DI Record Publish Date: September 24, 2016