Primary Device ID | 50884908005375 |
NIH Device Record Key | fcb0c640-098e-4f2d-8086-ff29bc0aa885 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TUNNELER |
Version Model Number | BTT |
Company DUNS | 038000253 |
Company Name | Medical Components, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com | |
Phone | +1(215)256-4201 |
clinical@medcompnet.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884908005370 [Primary] |
GS1 | 50884908005375 [Package] Contains: 00884908005370 Package: box [5 Units] In Commercial Distribution |
MZY | Graft,vascular,stainless steel tunneler |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-09-03 |
Device Publish Date | 2016-10-21 |
50884908031114 | 2- BARBED TUNNELERS FOR 6F PRO-LINE® |
50884908005375 | TESIO® BLUNT TUNNELER |