FDA UDI In Commercial Distribution 🇺🇸 United States

Prelivia

DI: 17540176050008 · Model: PR-IES1 · Rehabtronics Inc
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Prelivia
Primary DI
17540176050008
Version / Model
PR-IES1
Company Name
Rehabtronics Inc
Labeler DUNS
243936569
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-01
Public Version
2
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
1b1a6467-e5ac-4409-bf36-e02c63d7520c

Device Description

The Prelivia System is a portable transcutaneous muscle stimulation system intended to increase regional blood circulation at stimulated treatment areas, and to reduce the incidence and progression of pressure ulcers (bed sores) in individuals who are immobile due to their clinical condition. The system consists of a battery

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
No
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
IPF Stimulator, Muscle, Powered

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Primary 17540176050008

Premarket Submissions

Submission Number Supplement Number
K210979 000