| Primary Device ID | 50884908029395 |
| NIH Device Record Key | 477fe51a-53a2-4253-a202-6ae3b5f1dd77 |
| Commercial Distribution Discontinuation | 2017-06-21 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | CAVH Catheter |
| Version Model Number | MC5CAVH3 |
| Company DUNS | 038000253 |
| Company Name | Medical Components, 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 | true |
| 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(215)256-4201 |
| clinical@medcompnet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884908029390 [Primary] |
| GS1 | 50884908029395 [Package] Contains: 00884908029390 Package: box [5 Units] Discontinued: 2017-06-21 Not in Commercial Distribution |
| LFK | CATHETER, FEMORAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2015-10-23 |
| 50884908056186 | CAVH / CAVHD* CATHETER TRAY |
| 50884908055899 | 8F X 6" CAVH CATHETER TRAY |
| 50884908029975 | 8F X 15CM STRAIGHT C.A.V.H. CATHETER SET |
| 50884908029951 | 8F X 4-1/2" FLEXI CAVH CATHETER SET |
| 50884908029937 | 8F X 11.5CM STRAIGHT C.A.V.H. CATHETER SET |
| 50884908029715 | 7F X 11CM STRAIGHT CAVH CATHETER SET |
| 50884908029395 | 5F X 7.6CM CAVH CATHETER SET |