FDA UDI In Commercial Distribution 🇺🇸 United States

iSTIM

DI: 04719871184950 · Model: iSTIM PR-02-2 · EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iSTIM
Primary DI
04719871184950
Version / Model
iSTIM PR-02-2
Company Name
EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
Labeler DUNS
657383535
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-25
Public Version
1
Public Version Date
2023-09-04
Public Version Status
New
Public Device Record Key
8608b2d1-5392-4124-ac73-25457053dfc7

Device Description

Incontinence probe Perineal orifice incontinence-control electrical stimulation system electrode

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
Yes
MRI Safety
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
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
KPI Stimulator, Electrical, Non-Implantable, For Incontinence

GMDN Terms

Code Name
36050 Perineal orifice incontinence-control electrical stimulation system probe, reusable

Identifiers

Type ID
Primary 04719871184950

Premarket Submissions

Submission Number Supplement Number
K161349 000