Primary Device ID | 10607915119895 |
NIH Device Record Key | d7820fdb-6806-4db7-8669-c7a5fcc04de9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kii Optical Access System |
Version Model Number | CFR73 |
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 | 12 Millimeter |
Lumen/Inner Diameter | 12 Millimeter |
Lumen/Inner Diameter | 12 Millimeter |
Lumen/Inner Diameter | 12 Millimeter |
Length | 100 Millimeter |
Lumen/Inner Diameter | 12 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00607915119898 [Primary] |
GS1 | 10607915119895 [Package] Contains: 00607915119898 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 |