FDA UDI In Commercial Distribution 🇺🇸 United States

UpLyft

DI: 00860009140509 · Model: ST-120 · PATHWAY, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
UpLyft
Primary DI
00860009140509
Version / Model
ST-120
Company Name
PATHWAY, LLC
Labeler DUNS
080312381
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-08
Public Version
1
Public Version Date
2023-08-16
Public Version Status
New
Public Device Record Key
301ffdb8-70b2-4499-943f-064d3cd4cb2b

Device Description

Patient Transfer 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
No
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
12330 Mobile patient lifting system, electrically-powered

Identifiers

Type ID
Primary 00860009140509