| Primary Device ID | 08714729897279 |
| NIH Device Record Key | 3a390549-d13d-47fb-aa5b-529849a2cda3 |
| Commercial Distribution Discontinuation | 2021-01-19 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Symphion |
| Version Model Number | FG-0612-R |
| Company DUNS | 021717889 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 | 08714729897279 [Primary] |
| PGT | Insufflator, hysteroscopic, fluid, closed-loop recirculation with cutter-coagulator, endoscopic, bipolar |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2022-07-20 |
| Device Publish Date | 2016-09-24 |
| 08714729905806 | Tissue Removal System Refurbished 6.3 Endoscope |
| 08714729863670 | Tissue Removal System 6.3 Endoscope |
| 08714729897279 | Tissue Removal System Refurbished Controller |
| 08714729893318 | Tissue Removal System Spare Footswitch |
| 08714729863717 | Tissue Removal System Fluid Management Accessories |
| 08714729863687 | Tissue Removal System Controller |
| 08714729863656 | Tissue Removal System Resecting Device |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SYMPHION 85707057 4739444 Live/Registered |
Iogyn, Inc. 2012-08-17 |
![]() SYMPHION 75839291 2528275 Live/Registered |
SYMPHION, INC. 1999-11-03 |