Primary Device ID | 04042301144324 |
NIH Device Record Key | 7cc59412-1a12-4a9d-82d1-898029719c6b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TiMESH |
Version Model Number | 6000737 |
Company DUNS | 344675942 |
Company Name | pfm medical titanium gmbh |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04042301144317 [Primary] |
GS1 | 04042301144324 [Package] Contains: 04042301144317 Package: Box [3 Units] In Commercial Distribution |
OXJ | Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-17 |
Device Publish Date | 2019-12-09 |
04042301144348 | Ti-Mesh 1.4" X 4" Strong 65g/m² |
04042301144324 | Ti-Mesh 1.4" X 4" Light 35g/m² |
04042301097668 | Ti-Mesh 12" X 12" Light 35g/m² |
04042301097651 | Ti-Mesh 6" X 8" Light 35g/m² |
04042301097576 | Ti-Mesh 4" X 6" Light 35 g/m² |
04042301097552 | Ti-Mesh 4" X 6" Extra Light 16 g/m² |
04042301097606 | Ti-Mesh 6" X 6" Light 35g/m² |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TIMESH 75315249 2220142 Dead/Cancelled |
Sofamor Danek Properties, Inc. 1997-06-26 |
TIMESH 75102736 2047832 Live/Registered |
MEDTRONIC, INC. 1996-05-13 |
TIMESH 73662837 1492999 Dead/Cancelled |
TIMESH, INC. 1987-05-26 |