Primary Device ID | 00190837031329 |
NIH Device Record Key | 62c8638d-84c4-4bf9-adf5-990c79f23b62 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nautilus Non-Cannulated Iliac |
Version Model Number | 475-110-5 |
Catalog Number | 475-110-5 |
Company DUNS | 183641617 |
Company Name | Life Spine, 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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190837031329 [Primary] |
NKB | Thoracolumbosacral pedicle screw system |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
[00190837031329]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-15 |
Device Publish Date | 2019-11-07 |
00190837031367 | 485-110-5 |
00190837031350 | 485-105-5 |
00190837031343 | 485-100-5 |
00190837031336 | 485-95-5 |
00190837031329 | 475-110-5 |
00190837031312 | 475-105-5 |
00190837031305 | 475-100-5 |
00190837031299 | 475-95-5 |