| Primary Device ID | 00816728021094 |
| NIH Device Record Key | b5708275-2dfc-4323-aadf-f0721fe4226a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PhotonBlade™ |
| Version Model Number | PB1 |
| Catalog Number | PB1 |
| Company DUNS | 175697908 |
| Company Name | INVUITY, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 8667117768 |
| customerservice@invuity.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816728021094 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-04-24 |
| Device Publish Date | 2019-06-03 |
| 00816728020158 | he PhotonBlade is an RF device coupled with illumination that is indicated for cutting and coagu |
| 00816728021094 | he PhotonBlade is an RF device coupled with illumination that is indicated for cutting and coagu |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PHOTONBLADE 87017629 5210744 Live/Registered |
INVUITY, INC. 2016-04-28 |