| Primary Device ID | 00852503007167 |
| NIH Device Record Key | 8075e98f-ff8d-4caa-b59b-e7b2b2ebe182 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Venni / Biolight |
| Version Model Number | A5 |
| Company DUNS | 960516735 |
| Company Name | VENNI INSTRUMENTS 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00852503007167 [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 | 4 |
| Public Version Date | 2020-02-06 |
| Device Publish Date | 2016-10-06 |
| 00852503007211 | Venni / Biolight Fetal Monitor |
| 00852503007204 | Venni / Biolight Fetal Monitor |
| 00852503007198 | Venni / Biolight 12-channel EKG machine |
| 00852503007181 | Venni / Biolight 12-channel EKG machine |
| 00852503007174 | Venni / Biolight 3-channel EKG machine |
| 00852503007167 | Venni / Biolight 12.1" multi-parameter modular patient monitor |