| Primary Device ID | 00877972007043 |
| NIH Device Record Key | 5296d627-2ac2-45de-bde7-1367f87f5386 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GeniStrong |
| Version Model Number | 550-000-005G |
| Company DUNS | 079805400 |
| Company Name | GENICON, 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00877972007043 [Primary] |
| GCJ | Laparoscope, General & Plastic Surgery |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-08-16 |
| Device Publish Date | 2018-01-15 |
| 00877972007180 | 550-000-017G |
| 00877972007166 | 550-000-013G |
| 00877972007142 | 550-000-012G |
| 00877972007128 | 550-000-011G |
| 00877972007104 | 550-000-010G |
| 00877972007081 | 550-000-009G |
| 00877972007067 | 550-000-008G |
| 00877972007043 | 550-000-005G |
| 00877972007029 | 550-000-003G |
| 00877972005919 | 550-000-008 |
| 00877972005186 | 550-000-005 |
| 00877972004004 | 550-000-003 |