Primary Device ID | 00856233005073 |
NIH Device Record Key | 1956b9de-05bb-4a4e-85be-3b73141bbe92 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tapsystem |
Version Model Number | 2A Patient Cable |
Catalog Number | 2010 |
Company DUNS | 800214827 |
Company Name | CARDIOCOMMAND, 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 | true |
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 | (800) 231-6370 |
cconley@CardioCommand.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00856233005073 [Primary] |
LPA | System, Esophageal Pacing |
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 | 2015-07-22 |
00856233005158 | A pulse generator system for the treatment of cardiac dysrhythmias; re-manufactured, (unpackaged |
00856233005073 | A cable used to connect a patient to a Model 2A pulse generator system for the treatment of card |
00856233005066 | A pulse generator system for the treatment of cardiac dysrhythmias, (unpackaged unit). |