FDA UDI In Commercial Distribution 🇺🇸 United States

PRECISION TENS 3900

DI: 00816924020235 · Model: TENS3900V2 · Tensproducts, LLC
Product Codes
1
GMDN Terms
1
Identifiers
5
Pkg Device Count
1

Basic Information

Brand Name
PRECISION TENS 3900
Primary DI
00816924020235
Version / Model
TENS3900V2
Catalog Number
TENS3900V2, TENS3900-JETT, TENS3900-TP
Company Name
Tensproducts, LLC
Labeler DUNS
104307787
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-21
Public Version
5
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
06c083de-c968-48d9-9aca-d5805f88176a

Device Description

PRECISION TENS3900 4 MODE 90mA ANALOG TENS UNIT WITH TIMER

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
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 10816924020232
Package 00816924020433
Primary 00816924020235
Package 20816924020239
Package 00816924020716

Premarket Submissions

Submission Number Supplement Number
K003487 000