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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