Primary Device ID | 00888118026682 |
NIH Device Record Key | a29e5ef1-b318-4305-bbdd-f87d0d47db28 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GOUGE |
Version Model Number | 23-102-10-07 |
Company DUNS | 826499238 |
Company Name | KLS-Martin L.P. |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(904)641-7746 |
KLS-UDI-Info@klsmartin.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00888118026682 [Primary] |
GDH | GOUGE, SURGICAL, GENERAL & PLASTIC SURGERY |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00888118026682]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-08-21 |
Device Publish Date | 2018-09-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() GOUGE 85589295 4249788 Live/Registered |
Alfa-Row, Inc. 2012-04-04 |
![]() GOUGE 75682848 2332462 Dead/Cancelled |
Alfa-Row, Inc. 1999-04-12 |
![]() GOUGE 74660193 1953469 Dead/Cancelled |
Gouge Partnership 1995-04-07 |
![]() GOUGE 73497262 1332390 Dead/Cancelled |
Tomy Corporation 1984-08-30 |