Primary Device ID | 00850011929049 |
NIH Device Record Key | d1754d41-7d47-4441-be70-db988c6bf3b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SurgiMesh |
Version Model Number | Tintra E-1522 |
Company DUNS | 825244135 |
Company Name | BG MEDICAL, LLC |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850011929049 [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 | 2020-02-07 |
Device Publish Date | 2020-01-30 |
00850011929247 | T1418-8XD |
00850011929230 | T1116-8XD |
00850011929223 | T1115-8 |
00850011929216 | TEL613-8 |
00850011929209 | T613-8S |
00850011929193 | TEALFIL-8 |
00850011929186 | T3030 |
00850011929179 | T221510 |
00850011929155 | T1415 |
00850011929148 | T1015 |
00850011929131 | T510 |
00850011929124 | Tintra OK-1522 |
00850011929117 | Tintra OK-1015 |
00850011929100 | Tintra CK-10 |
00850011929094 | Tintra CK-7 |
00850011929070 | Tintra O-2636 |
00850011929063 | Tintra E-3030 |
00850011929056 | Tintra E-2226 |
00850011929049 | Tintra E-1522 |
00850011929032 | Tintra R-1415 |
00850011929025 | Tintra C-15 |
00850011929018 | Tintra C-12 |
00850011929001 | Tintra C-10 |
00850011929292 | T5050 |
00850011929278 | T4040 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SURGIMESH 78596819 3092701 Live/Registered |
ASPIDE MEDICAL 2005-03-29 |
SURGIMESH 76322955 2762499 Dead/Cancelled |
HOWMEDICA OSTEONICS CORP. 2001-10-09 |