FDA UDI In Commercial Distribution 🇺🇸 United States

PainAway Pro

DI: 00822383549460 · Model: RTLAGF-940 · Drive Devilbiss Healthcare
Product Codes
2
GMDN Terms
4
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
PainAway Pro
Primary DI
00822383549460
Version / Model
RTLAGF-940
Company Name
Drive Devilbiss Healthcare
Labeler DUNS
867673159
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-01
Public Version
7
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
f0a37258-c017-46c1-86ac-4befb1af5290

Device Description

2" Round Long Lasting Electrodes

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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NGX STIMULATOR, MUSCLE, POWERED, FOR MUSCLE CONDITIONING
NUH STIMULATOR, NERVE, TRANSCUTANEOUS, OVER-THE-COUNTER

GMDN Terms

Code Name
35372 Analgesic transcutaneous electrical nerve stimulation system
35995 Transcutaneous electrical stimulation electrode, single-use
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system
35751 Transcutaneous electrical stimulation lead

Identifiers

Type ID
Package 50822383549465
Package 10822383549467
Primary 00822383549460