| Primary Device ID | 07350021982209 |
| NIH Device Record Key | 1eefc093-fa36-4a39-aa0c-30c85315a5f1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Double Pump Patient cassette |
| Version Model Number | 1002059 |
| Company DUNS | 508778565 |
| Company Name | Medical Vision AB |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 07350021982001 [Primary] |
| GS1 | 07350021982100 [Package] Contains: 07350021982001 Package: [10 Units] In Commercial Distribution |
| GS1 | 07350021982209 [Package] Contains: 07350021982100 Package: [2 Units] In Commercial Distribution |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-04-23 |
| Device Publish Date | 2016-09-24 |
| 17350021987003 - PowerPumpTM dp System Day Cassette | 2019-04-23 |
| 17350021987027 - PowerPumpTM dp System Patient cassette | 2019-04-23 |
| 17350021987058 - PowerPumpTM dp System Patient tubing | 2019-04-23 |
| 07350021981202 - Double Pump Day cassette/ Double Pump RF Day cassette | 2019-04-23 |
| 07350021981523 - Double Pump Single/ Double Pump RF Single | 2019-04-23 |
| 07350021982209 - Double Pump Patient cassette | 2019-04-23 |
| 07350021982209 - Double Pump Patient cassette | 2019-04-23 |
| 07350021982704 - Double Pump RF Patient cassette | 2019-04-23 |
| 17350021986105 - PowerPumpTM dp System | 2018-07-06 |