| Primary Device ID | 00852132007316 |
| NIH Device Record Key | 04e10ae4-4f40-49d3-b18d-fe8b173f471b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PatientCare Link |
| Version Model Number | SW1004 |
| Company DUNS | 859807815 |
| Company Name | PREVENTICE TECHNOLOGIES, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00852132007316 [Primary] |
| DSI | Detector And Alarm, Arrhythmia |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-24 |
| Device Publish Date | 2021-06-16 |
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