Primary Device ID | 04538612903571 |
NIH Device Record Key | 789dc5b4-0ea8-4595-9909-4fa3616c8ecc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FUKUDA DENSHI |
Version Model Number | CMF-700-3FA |
Company DUNS | 690671011 |
Company Name | FUKUDA DENSHI CO.,LTD. |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04538612903571 [Primary] |
MHX | Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-01-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FUKUDA DENSHI 75500255 2346482 Live/Registered |
FUKUDA DENSHI CO., LTD. 1998-06-11 |
![]() FUKUDA DENSHI 73433851 1351395 Dead/Cancelled |
FUKUDA DENSHI KABUSHIKI KAISHA 1983-07-11 |