FDA UDI In Commercial Distribution 🇺🇸 United States

Revi™ Implant

DI: 07290017912011 · Model: MA-1007-0600_US_CM · BLUEWIND MEDICAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Revi™ Implant
Primary DI
07290017912011
Version / Model
MA-1007-0600_US_CM
Company Name
BLUEWIND MEDICAL LTD
Labeler DUNS
534159913
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-15
Public Version
1
Public Version Date
2023-09-25
Public Version Status
New
Public Device Record Key
2acc7d6c-fe2e-4f8c-b92e-3cc643cd1dde

Device Description

Implantable, wireless, battery-less neurostimulation component of the Revi Peripheral Nerve Stimulation System

Device Characteristics

Single Use
Yes
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QXM Implanted Tibial Electrical Urinary Continence Device

GMDN Terms

Code Name
64780 Tibial nerve implantable incontinence-control electrical stimulation system

Identifiers

Type ID
Primary 07290017912011

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
DEN220073 000