FDA UDI In Commercial Distribution 🇺🇸 United States

TensCare

DI: 05033435133796 · Model: Shockwave · TENSCARE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TensCare
Primary DI
05033435133796
Version / Model
Shockwave
Catalog Number
K-SHOCKWAVE
Company Name
TENSCARE LIMITED
Labeler DUNS
569403736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-08
Public Version
2
Public Version Date
2023-10-12
Public Version Status
Update
Public Device Record Key
629f44b1-d988-477c-8a7e-9d517bd88817

Device Description

Shockwave is a solenoid drive activates a bullet body inside the therapeutic handle. When the bullet body collides with the therapeutic head, the impact energy is converted into a radial ballistic shock wave pulse, which is focussed to create the characteristics required to have a good therapeutic effect for musculoskeletal disorders. The innovative technology has a compact design with no need for a compressor. The clear colour display shows all relevant treatment parameters and offers touch screen operation for ease of use during treatment. Variable frequencies and various applicator heads allow treatment to be adapted to the particular condition of the patient.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
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
ISA Massager, Therapeutic, Electric

GMDN Terms

Code Name
47790 Electromechanical orthopaedic extracorporeal shock wave therapy system

Identifiers

Type ID
Primary 05033435133796