FDA UDI In Commercial Distribution 🇺🇸 United States

Ignite MD

DI: 00850998008997 · Model: Manaflexx2 · MANAMED INC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ignite MD
Primary DI
00850998008997
Version / Model
Manaflexx2
Catalog Number
MF002-RX
Company Name
MANAMED INC
Labeler DUNS
084042331
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-23
Public Version
3
Public Version Date
2023-11-07
Public Version Status
Update
Public Device Record Key
d471c684-5b09-4ba8-a5b0-efff19e0919b

Device Description

ManaFlexx 2 is the only NMES device designed for ease of use by eliminating wires or standalone electrodes. This device is single patient use and is designed for use in the home to treat muscle atrophy due to lack of use or surgery. Powered muscle stimulators should only be used under medical supervision for adjunctive therapy for the treatment of medical diseases and conditions Completely portable no wires or bulky devices Can be placed anywhere treatment is desired Battery operated Reusable - simply replace pads and batteries

Device Characteristics

Single Use
No
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
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
NYN Stimulator, Electrical, Transcutaneous, For Arthritis
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
IPF Stimulator, Muscle, Powered

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00850998008997

Customer Contacts

Phone
888-508-0712