FDA UDI In Commercial Distribution 🇺🇸 United States

FlexPlus

DI: 10185098000754 · Model: ProM-028 · PRO MEDICAL SUPPLIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
200

Basic Information

Brand Name
FlexPlus
Primary DI
10185098000754
Version / Model
ProM-028
Catalog Number
ProM-028
Company Name
PRO MEDICAL SUPPLIES, INC.
Labeler DUNS
135741127
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2016-07-26
Public Version
4
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
648cd2c9-c504-44e0-aa92-1c17e0a8eede

Device Description

Electrodes Black Foam 1.75"x3.75" (50 packs per case-4 electrodes per pack = 200)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXY Electrode, Cutaneous

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Primary 10185098000754
Unit of Use 18509800075720

Customer Contacts

Phone
215-938-0200

Premarket Submissions

Submission Number Supplement Number
K132998 000