Primary Device ID | 20705031206455 |
NIH Device Record Key | ceb8410d-e1b3-4f43-901b-1ebea2cf8b20 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ENDOKNOT |
Version Model Number | JK10G |
Catalog Number | JK10G |
Company DUNS | 002144145 |
Company Name | ETHICON 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 | +1(877)384-4266 |
xxx@xxx.xxx | |
Phone | +1(877)384-4266 |
xxx@xxx.xxx | |
Phone | +1(877)384-4266 |
xxx@xxx.xxx | |
Phone | +1(877)384-4266 |
xxx@xxx.xxx | |
Phone | +1(877)384-4266 |
xxx@xxx.xxx | |
Phone | +1(877)384-4266 |
xxx@xxx.xxx | |
Phone | +1(877)384-4266 |
xxx@xxx.xxx | |
Phone | +1(877)384-4266 |
xxx@xxx.xxx | |
Phone | +1(877)384-4266 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10705031206458 [Primary] |
GS1 | 20705031206455 [Package] Contains: 10705031206458 Package: BOX [12 Units] In Commercial Distribution |
GAM | SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2021-02-05 |
Device Publish Date | 2015-09-24 |
20705031206493 | ENDOKNOT PDS*II VL MONO DOM PRT - 3PL |
20705031206455 | ENDOKNOT VL CT VCL |
20705031206400 | ENDOKNOT ETHIBOND VD 0 107CM AG ST3 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ENDOKNOT 74261885 1748324 Dead/Cancelled |
JOHNSON & JOHNSON 1992-04-02 |