FDA UDI Not in Commercial Distribution 🇺🇸 United States

Pain Remedy

DI: 00782944027007 · Model: C05W · Hi-Dow International Incorporated
Product Codes
2
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pain Remedy
Primary DI
00782944027007
Version / Model
C05W
Company Name
Hi-Dow International Incorporated
Labeler DUNS
124034476
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-10
Public Version
10
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
0883b74b-66f7-44e7-aa42-83ccc9966383
Distribution End Date
2021-03-02

Device Description

Electronic Muscle Stimulator

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
Yes
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
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system
35372 Analgesic transcutaneous electrical nerve stimulation system
35751 Transcutaneous electrical stimulation lead

Identifiers

Type ID
Primary 00782944027007