FDA UDI In Commercial Distribution 🇺🇸 United States

Tenscare

DI: 05033435134458 · Model: Sure+ · TENSCARE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tenscare
Primary DI
05033435134458
Version / Model
Sure+
Catalog Number
K-SURE+USA
Company Name
TENSCARE LIMITED
Labeler DUNS
569403736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-28
Public Version
1
Public Version Date
2019-12-06
Public Version Status
New
Public Device Record Key
a3c0c88a-6dbe-4ea7-8857-a6e453e2cccb

Device Description

The Sure + is intended to provide electrical stimulation and neuromuscular re-education for the purpose of rehabilitation of weak pelvic floor muscles for the treatment of stress, urge, and mixed urinary incontinence in women and to maintain urinary continence in women. The Sure + is intended for OTC use.

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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
36784 Perineal orifice incontinence-control electrical stimulation system

Identifiers

Type ID
Primary 05033435134458

Customer Contacts

Phone
800 308 7390

Premarket Submissions

Submission Number Supplement Number
K191312 000