FDA UDI In Commercial Distribution 🇺🇸 United States

LiftWalk

DI: 00860014768668 · Model: Plus · INNOMOTIVE L.L.C
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LiftWalk
Primary DI
00860014768668
Version / Model
Plus
Company Name
INNOMOTIVE L.L.C
Labeler DUNS
122432830
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-04
Public Version
1
Public Version Date
2026-02-12
Public Version Status
New
Public Device Record Key
b2ed1f39-8e53-4576-bc02-957f60b88422

Device Description

Non-AC powered patient lift system.

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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FSA Lift, Patient, Non-Ac-Powered

GMDN Terms

Code Name
45678 Mobile patient lifting system, manual

Identifiers

Type ID
Primary 00860014768668