Primary Device ID | 00887517397881 |
NIH Device Record Key | ba83a9c2-68f1-40b4-8d8d-85853084990a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Graft Delivery System |
Version Model Number | 5019008 |
Company DUNS | 053950783 |
Company Name | Nuvasive, 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 | true |
OTC Over-The-Counter | false |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887517397881 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887517397881]
Moist Heat or Steam Sterilization
[00887517397881]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-25 |
Device Publish Date | 2018-09-24 |
00887517518873 | Graft Delivery System |
00887517452719 | GDS Graft Pusher |
00887517397898 | GDS Graft Pusher |
00887517397881 | GDS K-Wire, Funnel Cap |
00887517397867 | GDS Graft Funnel |
00887517397829 | GDS Graft Tube |
00887517213136 | GDS Counter-Torque |
00887517213129 | GDS Graft Pusher |
00887517212696 | GDS Graft Removal Tool |
00887517707505 | GDS Tube, Tapered Small |
00887517707482 | GDS Tube, 8.4mm Curved |
00887517707475 | GDS Tube, 7.5mm Curved |
00887517707499 | GDS Applicator, Ø5mm Threaded |