Primary Device ID | 10607915116047 |
NIH Device Record Key | 2d71b46b-d699-4ceb-a455-2a1b90f1bf00 |
Commercial Distribution Discontinuation | 2016-08-12 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Kii® Sheilded Bladed Access Sysem |
Version Model Number | C0Q51 |
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 | false |
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 | 55 Millimeter |
Lumen/Inner Diameter | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00607915116040 [Primary] |
GS1 | 10607915116047 [Package] Contains: 00607915116040 Package: [6 Units] Discontinued: 2016-08-12 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 | 2016-08-12 |
10607915116146 | Trocar |
10607915116139 | Trocars |
10607915116054 | Trocars |
10607915116047 | Trocars |
10607915116023 | Trocars |
10607915116016 | Trocars |