Primary Device ID | 04931921899359 |
NIH Device Record Key | ec222d11-6265-4acb-be25-ae9d27f23de1 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | YP-710T |
Catalog Number | YP-710T |
Company DUNS | 690568050 |
Company Name | NIHON KOHDEN CORPORATION |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com | |
Phone | +1(800)325-0283 |
info@nkusa.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04931921899359 [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 | 2019-07-22 |
Device Publish Date | 2016-09-05 |
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04931921010235 - cap-ONE | 2023-05-30 cap-ONE Nasal Adapter, Adult |
04931921010273 - cap-ONE | 2023-05-30 cap-ONE Nasal Adapter, Adult, w/ Oxygen tube |