FDA UDI In Commercial Distribution 🇺🇸 United States

Pure Impact

DI: 07290018152164 · Model: KT00040 · SOFWAVE MEDICAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pure Impact
Primary DI
07290018152164
Version / Model
KT00040
Catalog Number
KT00040
Company Name
SOFWAVE MEDICAL LTD
Labeler DUNS
531962539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-01
Public Version
1
Public Version Date
2026-02-09
Public Version Status
New
Public Device Record Key
69eff0f4-0b23-4674-b13b-b0caa5e47389

Device Description

Powered Muscle Stimulator (EMS) KIT. The KIT contains 3 components (all individually registered in GUDID): (SN) FG00013 with UDI: 07290018152133 (SN) FG00014 with UDI: 07290018152140 (SN) FG00015 with UDI: 17290018152154

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
MR Unsafe
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 07290018152164

Premarket Submissions

Submission Number Supplement Number
K232455 000
K241685 000
K250146 000
K251746 000

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Storage Environment Humidity
Temperature Range
30 – 70 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius