FDA UDI In Commercial Distribution 🇺🇸 United States

TENS 3000

DI: 00813520010776 · Model: DT3002 · COMPASS HEALTH BRANDS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TENS 3000
Primary DI
00813520010776
Version / Model
DT3002
Company Name
COMPASS HEALTH BRANDS CORP.
Labeler DUNS
827221698
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-12
Public Version
9
Public Version Date
2023-09-14
Public Version Status
Update
Public Device Record Key
f257cebe-2cfb-475e-bc1b-af0e253c3854

Device Description

TENS 3000 Analog

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Package 80813520010772
Primary 00813520010776

Customer Contacts

Phone
800-376-7263

Premarket Submissions

Submission Number Supplement Number
K102014 000