| Primary Device ID | 10607915116092 |
| NIH Device Record Key | 4253020a-ee7c-41dc-b723-5071b7584fe6 |
| Commercial Distribution Discontinuation | 2016-08-16 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Kii® Sheilded Bladed Dual Pack |
| Version Model Number | C0Q56 |
| 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 | 5 Millimeter |
| Lumen/Inner Diameter | 5 Millimeter |
| Lumen/Inner Diameter | 5 Millimeter |
| Lumen/Inner Diameter | 5 Millimeter |
| Length | 150 Millimeter |
| Lumen/Inner Diameter | 5 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00607915116095 [Primary] |
| GS1 | 10607915116092 [Package] Contains: 00607915116095 Package: [10 Units] Discontinued: 2016-08-16 Not 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 | 4 |
| Public Version Date | 2020-01-29 |
| Device Publish Date | 2016-08-16 |
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