| Primary Device ID | 00850033976090 |
| NIH Device Record Key | fd584ad3-8849-4f92-965a-700fa0b7674b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Symphion Controller |
| Version Model Number | FG-0612 |
| Catalog Number | FG-0612 |
| Company DUNS | 829616478 |
| Company Name | Minerva Surgical, Inc. |
| 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 | 00850033976090 [Primary] |
| GS1 | 08714729863687 [Previous] |
| PGT | Insufflator, Hysteroscopic, Fluid, Closed-Loop Recirculation With Cutter-Coagulator, Endoscopic, Bipolar |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-11 |
| Device Publish Date | 2022-05-03 |
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