| Primary Device ID | 08031527014883 |
| NIH Device Record Key | eb063b4a-4fc8-4a91-80c5-e7896baaac0d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SPIDERVIEW+ SD MEMORY CARD |
| Version Model Number | SD Card |
| Company DUNS | 434932033 |
| Company Name | SORIN GROUP ITALIA SRL |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08031527014883 [Primary] |
| MWJ | ELECTROCARDIOGRAPH,AMBULATORY(WITHOUT ANALYSIS) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2016-09-22 |
| 38033178004009 - Aortic-Root Cannula | 2025-04-17 |
| 38033178004016 - Aortic-Root Cannula | 2025-04-17 |
| 38033178004023 - Aortic-Root Cannula | 2025-04-17 |
| 38033178004030 - Aortic-Root Cannula | 2025-04-17 |
| 38033178004047 - Aortic-Root Cannula | 2025-04-17 |
| 38033178004054 - Aortic-Root Cannula | 2025-04-17 |
| 38033178114562 - MICRO | 2025-03-12 |
| 38033178114579 - MICRO | 2025-03-12 |