FDA UDI In Commercial Distribution 🇺🇸 United States

HiDow

DI: 00810093080373 · Model: HD-19A-RECEIVER · Hi-Dow International Incorporated
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HiDow
Primary DI
00810093080373
Version / Model
HD-19A-RECEIVER
Company Name
Hi-Dow International Incorporated
Labeler DUNS
124034476
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-22
Public Version
1
Public Version Date
2024-10-30
Public Version Status
New
Public Device Record Key
fe060c04-2d1e-4f0b-a646-2fb042f7cf1a

Device Description

Universal Receiver

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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
GXY Electrode, Cutaneous

GMDN Terms

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

Identifiers

Type ID
Primary 00810093080373

Premarket Submissions

Submission Number Supplement Number
K233461 000