| Primary Device ID | 00884838054943 | 
| NIH Device Record Key | b63c753b-1990-4cac-8173-e9dec66aeca6 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Expression MR ECG Leads, IEC, Neonatal | 
| Version Model Number | 989803193771 | 
| Catalog Number | 989803193771 | 
| Company DUNS | 013649151 | 
| Company Name | INVIVO CORPORATION | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Conditional | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | false | 
| Lot Batch | false | 
| Serial Number | true | 
| 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 | 
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | |
| Phone | +1(999)999-9999 | 
| xx@xx.xx | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00884838054943 [Primary] | 
| MWI | MONITOR,PHYSIOLOGICAL,PATIENT(WITHOUT 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 | 2016-10-05 | 
| 00884838103740 - Sentinelle | 2023-03-06 Sentinelle, Biopsy Grid | 
| 00884838115279 - Invivo | 2022-11-30 Kit, Enhanced Access, Bilateral Upgrade consists of Fiducial Marker Block; 3 Grid Plates Enhanced Access-Lateral; 3 Grid Plates | 
| 00884838115309 - Invivo | 2022-11-30 dS Breast 16 Biopsy Pack, 1.5T contains - 4 Lateral Grids Upper dS Breast 16Ch I/T; 4 Medial Grids dS Breast 16CH I/T; MRI Needl | 
| 00884838115255 - Invivo | 2022-11-28 BREAST 7 BIOPSY PACK 1.5T contains - 3 LBS M-L Grid Immobilization Plates; 3 LBS M-L Pillar Immobilization Plates Sterilized; M | 
| 00884838115507 - Sentinelle | 2022-10-24 DS Sentinelle Breast 16CH Coil Kit, 1.5T Consists of 1CH Left and Right Lateral Coils and Medial Plug with box of 10 Sentinelle | 
| 00884838115514 - Sentinelle | 2022-10-24 DS Sentinelle Breast coil, Biopsy Kit 3.0T Consists of 1CH Left and Right Lateral Coils and Medial Plug with box of 10 Sentinell | 
| 00884838105195 - Sentinelle | 2022-10-20 dS 3.0T 4CH Lateral Left | 
| 00884838105201 - Sentinelle | 2022-10-20 dS 3.0T 4CH Lateral Right |