Primary Device ID | 00841668114766 |
NIH Device Record Key | 26770207-c792-40bd-a3ba-af2404ad76ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DuraPlug |
Version Model Number | 0077 |
Catalog Number | 0077 |
Company DUNS | 085668598 |
Company Name | KATENA PRODUCTS, INC. |
Device Count | 1 |
DM Exempt | true |
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 | (973) 989-1600 |
globe@katena.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841668114766 [Primary] |
LZU | Plug, Punctum |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-03-31 |
00841668114773 | DuraPlug 0.4mm D x 2.0mm L - 2/Pkg, 10 Pkg/Box |
00841668114766 | DuraPlug 0.3mm D x 2.0mm L - 2/Pkg, 10 Pkg/Box |
00841668114759 | DuraPlug 0.2mm D x 2.0mm L - 2/Pkg, 10 Pkg/Box |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DURAPLUG 78570293 3276631 Live/Registered |
KATENA PRODUCTS, INC. 2005-02-18 |
![]() DURAPLUG 75960485 not registered Dead/Abandoned |
ALCON, INC. 2000-03-16 |