Primary Device ID | 10603295125914 |
NIH Device Record Key | 2c572171-e8b9-4ec2-9bfa-7e25d7bd1103 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LEGEND II |
Version Model Number | 2490-90-000 |
Catalog Number | 249090000 |
Company DUNS | 080506581 |
Company Name | DEPUY ORTHOPAEDICS, INC. |
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 | false |
OTC Over-The-Counter | false |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10603295125914 [Primary] |
FZY | HAMMER, SURGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10603295125914]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2018-09-24 |
10603295125914 | LEGEND II SLAP HAMMER EXTRACTOR |
10603295125952 | LEGEND II FIXATION PIN .125in x 3in |
10603295125853 | LEGEND II .125DRILL W/DEPTH STOP |
10603295125884 | LEGEND II PROXIMAL TIBIA RESECTION GDE |
10603295125877 | LEGEND II IM ALIGNMENT ROD TIBIAL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LEGEND II 74249009 1759711 Dead/Cancelled |
Medtronic, Inc. 1992-02-24 |