FDA UDI Not in Commercial Distribution 🇺🇸 United States

LiftMate

DI: 00728564000006 · Model: 3000 · The Brewer Company LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LiftMate
Primary DI
00728564000006
Version / Model
3000
Catalog Number
3000
Company Name
The Brewer Company LLC
Labeler DUNS
006073399
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2022-12-13
Public Version Status
Update
Public Device Record Key
7b88deef-cc34-4e3a-9a92-570b1bc42f04
Distribution End Date
2018-10-17

Device Description

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

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FNG Lift, Patient, Ac-Powered

GMDN Terms

Code Name
30021 Freestanding patient lifting system, electrically-powered

Identifiers

Type ID
Primary 00728564000006

Customer Contacts

Phone
888-273-9371