| Primary Device ID | 10607915123229 |
| NIH Device Record Key | c8f45b1c-1d5b-420f-8262-907400bb4352 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kii Optical Access System |
| Version Model Number | CFR33 |
| Company DUNS | 187129135 |
| Company Name | APPLIED MEDICAL RESOURCES CORPORATION |
| 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 | 1.949.713.8300 |
| contact@appliedmedical.com | |
| Phone | 1.949.713.8300 |
| contact@appliedmedical.com | |
| Phone | 1.949.713.8300 |
| contact@appliedmedical.com |
| Lumen/Inner Diameter | 11 Millimeter |
| Lumen/Inner Diameter | 11 Millimeter |
| Lumen/Inner Diameter | 11 Millimeter |
| Lumen/Inner Diameter | 11 Millimeter |
| Length | 100 Millimeter |
| Lumen/Inner Diameter | 11 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00607915123222 [Primary] |
| GS1 | 10607915123229 [Package] Contains: 00607915123222 Package: [6 Units] In Commercial Distribution |
| 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 | 3 |
| Public Version Date | 2020-01-09 |
| Device Publish Date | 2016-09-13 |
| 10607915125742 | Trocar |
| 10607915125735 | Trocar |
| 10607915123229 | Trocar |
| 10607915123038 | Trocar |
| 10607915122291 | Trocar |
| 10607915119956 | Trocar |
| 10607915119895 | Trocar |
| 10607915119888 | Trocar |
| 10607915140172 | Trocar |