Primary Device ID | B312F4047PF0 |
NIH Device Record Key | 3d68ef98-8b0e-4b78-a09c-0f0a5512822f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProFlex |
Version Model Number | F5047PF |
Company DUNS | 245449335 |
Company Name | C.M.P. Canadian Medical Products Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B312F4047PF0 [Primary] |
GXY | Electrode, Cutaneous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-22 |
Device Publish Date | 2022-08-12 |
B312F5047PF0 | ProFlex Sport Electrode - 1.8" x 1.8" Square 4/pk |
B312F4047PF0 | PROFLEX AgC REUSABLE ELECTRODES - 2 X 2" SQUARE 4/pk |