| Primary Device ID | 00884838032507 |
| NIH Device Record Key | f37f4c67-e20c-405e-b330-8b57ca2c0e8f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CABLE,FIBER OPTIC VCG |
| Version Model Number | 452215033602 |
| Catalog Number | 452215033602 |
| Company DUNS | 013649151 |
| Company Name | INVIVO 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 | false |
| OTC Over-The-Counter | false |
| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884838032507 [Primary] |
| MWI | Monitor, physiological, patient (without arrhythmia detection or alarms) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-30 |
| Device Publish Date | 2019-04-22 |
| 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 |