| Primary Device ID | 50884908026752 |
| NIH Device Record Key | 769b16ef-d3a9-4b54-a195-153612d2759c |
| Commercial Distribution Discontinuation | 2018-06-29 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | STRAIGHT FEMORAL |
| Version Model Number | MCF64 |
| 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 | 00884908026757 [Primary] |
| GS1 | 50884908026752 [Package] Contains: 00884908026757 Package: box [10 Units] Discontinued: 2018-06-29 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 | 4 |
| Public Version Date | 2019-12-11 |
| Device Publish Date | 2015-11-17 |
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