Primary Device ID | 00613994533265 |
NIH Device Record Key | c12e8b71-0806-434d-8a7a-fedd719ee5f7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PACEART® SYSTEM GET CONNECTED III |
Version Model Number | PASTCGCIII |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, 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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994533265 [Primary] |
DPS | ELECTROCARDIOGRAPH |
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 | 2016-04-01 |
00613994845801 | SW PASDEVUGCIII PACEART GLBL MR V 2.0 |
00613994533364 | SW PASCLGCIII PACEART GLBL MR GCIII |
00613994533333 | SW PASDEMOGCIII PACEART GLBL MR GCIII |
00613994533319 | SW PASDOCGCIII PACEART GLBL MR GCIII |
00613994533302 | SW PASEXPGCIII PACEART GLBL MR GCIII |
00613994533296 | SW PASGATEGCIII PACEART GLBL MR GCIII |
00613994533272 | SW PASSATGCIII PACEART GLBL MR GCIII |
00613994533265 | SW PASTCGCIII PACEART GLBL MR GCIII |
00613994533241 | SW PASTMGCIII PACEART GLBL MR GCIII |
00643169357730 | SW PASDEVU3 DEV UPDATE MKT GLBL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PACEART 87252084 5195774 Live/Registered |
Medtronic, Inc. 2016-11-30 |
PACEART 74074454 1650680 Live/Registered |
Paceart, Inc. 1990-07-02 |