| Primary Device ID | 07612367053174 |
| NIH Device Record Key | 2fcb2a99-9b54-4947-bc12-80c28f7b9ee8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Invia Motion 60 Days |
| Version Model Number | 200.8591 |
| Company DUNS | 488293218 |
| Company Name | Medela AG |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| Manufacturing Date | true |
| 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 | 07612367053174 [Primary] |
| GS1 | 07612367089081 [Direct Marking] |
| OMP | Negative Pressure Wound Therapy Powered Suction Pump |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-06-07 |
| 07612367053174 | Negative Pressure Wound Therapy System / 087.4014 |
| 07612367026260 | Negative Pressure Wound Therapy System / 087.4000 |