FDA UDI In Commercial Distribution 🇺🇸 United States

TENS 7000

DI: 00023601680372 · Model: DT7202-16 · COMPASS HEALTH BRANDS CORP.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
TENS 7000
Primary DI
00023601680372
Version / Model
DT7202-16
Company Name
COMPASS HEALTH BRANDS CORP.
Labeler DUNS
827221698
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-29
Public Version
1
Public Version Date
2024-11-06
Public Version Status
New
Public Device Record Key
a5368915-eb94-4bb7-9c51-6539168d7ba1

Device Description

TENS 7000 w 16 pk

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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

Identifiers

Type ID
Package 80023601680378
Primary 00023601680372

Customer Contacts

Phone
800-376-7263