Primary Device ID | 00850002394078 |
NIH Device Record Key | 395d31cd-5f36-4c13-b9d3-cb4ac27a6911 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | T-Line Hernia Mesh |
Version Model Number | TL3020 |
Catalog Number | TL3020 |
Company DUNS | 079752359 |
Company Name | Deep Blue Medical Advances, 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 | 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 | 833-833-3275 |
cs@deepbluemedical.com | |
Phone | 833-833-3275 |
cs@deepbluemedical.com | |
Phone | 833-833-3275 |
cs@deepbluemedical.com | |
Phone | 833-833-3275 |
cs@deepbluemedical.com | |
Phone | 833-833-3275 |
cs@deepbluemedical.com | |
Phone | 833-833-3275 |
cs@deepbluemedical.com | |
Phone | 833-833-3275 |
cs@deepbluemedical.com | |
Phone | 833-833-3275 |
cs@deepbluemedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850002394078 [Primary] |
FTL | Mesh, Surgical, Polymeric |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-09 |
Device Publish Date | 2020-10-30 |
00850002394078 | T-Line Hernia Mesh, 29cm x 20.5cm |
00850002394061 | T-Line Hernia Mesh, 29cm x 15.5cm |
00850002394054 | T-Line Hernia Mesh, 29cm x 10.5cm |
00850002394047 | T-Line Hernia Mesh, 29cm x 5.5cm |
00850002394030 | T-Line Hernia Mesh, 13.5cm x 20.5cm |
00850002394023 | T-Line Hernia Mesh, 13.5cc x 15.5cm |
00850002394016 | T-Line Hernia Mesh, 13.5cm x 10.5cm |
00850002394009 | T-Line Hernia Mesh, 13.5cm x 5.5cm |