Primary Device ID | 00887517304537 |
NIH Device Record Key | 3ee81445-033d-45f0-84a9-5a462f611575 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Archon |
Version Model Number | 8880517 |
Company DUNS | 053950783 |
Company Name | Nuvasive, 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 | 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 | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com | |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887517304537 [Primary] |
KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
[00887517304537]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-04-09 |
Device Publish Date | 2015-10-24 |
00887517517074 | Beta Archon ACP |
00887517516305 | Archon Reconstructive 5 Level Set |
00887517516299 | Archon Reconstructive 4 Level Set |
00887517516282 | Archon Reconstructive 2 and 3 Level Set |
00887517516275 | Archon ACP Instrument System |
00887517516268 | Archon ACP Implant 5L System |
00887517516251 | Archon ACP Implant 4L System |
00887517516244 | Archon ACP Implant System |
00887517516237 | Archon Bicortical Drill Guide Set |
00887517514868 | Alpha Archon Reconstructive Set |
00887517514851 | Alpha Archon ACP System |
00887517499554 | Archon Screw, Ø4.0x23mm SD Fixed |
00887517499547 | Archon Screw, Ø4.0x22mm SD Fixed |
00887517499530 | Archon Screw, Ø4.0x21mm SD Fixed |
00887517499523 | Archon Screw, Ø4.0x20mm SD Fixed |
00887517499516 | Archon Screw, Ø4.0x19mm SD Fixed |
00887517499509 | Archon Screw, Ø4.0x18mm SD Fixed |
00887517499493 | Archon Screw, Ø4.0x17mm SD Fixed |
00887517499486 | Archon Screw, Ø4.0x16mm SD Fixed |
00887517499479 | Archon Screw, Ø4.0x15mm SD Fixed |
00887517499462 | Archon Screw, Ø4.0x14mm SD Fixed |
00887517499455 | Archon Screw, Ø4.0x13mm SD Fixed |
00887517499448 | Archon Screw, Ø4.0x12mm SD Fixed |
00887517499431 | Archon Screw, Ø4.0x11mm SD Fixed |
00887517499424 | Archon Screw, Ø4.0x10mm SD Fixed |
00887517380180 | Archon Plate Holder, Screw Hole |
00887517342447 | Archon Guide, Plate Holding DTS Mid |
00887517342430 | Archon Guide, Plate Holding DTS End |
00887517341976 | Archon Driver, Ball Detent |
00887517335753 | Archon Plate, 70mm 3-Level BETA |
00887517335746 | Archon Plate, 69mm 3-Level BETA |
00887517335739 | Archon Plate, 68mm 3-Level BETA |
00887517335722 | Archon Plate, 67mm 3-Level BETA |
00887517335715 | Archon Plate, 66mm 3-Level BETA |
00887517335708 | Archon Plate, 65mm 3-Level BETA |
00887517335395 | Archon Plate, 64mm 3-Level BETA |
00887517335388 | Archon Plate, 63mm 3-Level BETA |
00887517335371 | Archon Plate, 62mm 3-Level BETA |
00887517335364 | Archon Plate, 61mm 3-Level BETA |
00887517335357 | Archon Plate, 60mm 3-Level BETA |
00887517335340 | Archon Plate, 59mm 3-Level BETA |
00887517335333 | Archon Plate, 58mm 3-Level BETA |
00887517335326 | Archon Plate, 57mm 3-Level BETA |
00887517335319 | Archon Plate, 56mm 3-Level BETA |
00887517335302 | Archon Plate, 55mm 3-Level BETA |
00887517334695 | Archon Plate, 54mm 3-Level BETA |
00887517334688 | Archon Plate, 53mm 3-Level BETA |
00887517334671 | Archon Plate, 52mm 3-Level BETA |
00887517334664 | Archon Plate, 51mm 3-Level BETA |
00887517334657 | Archon Plate, 50mm 3-Level BETA |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ARCHON 98443747 not registered Live/Pending |
CRÃZR SADDLES, LLC 2024-03-11 |
ARCHON 90733868 not registered Live/Pending |
ID Technologies, LLC 2021-05-25 |
ARCHON 90237699 not registered Live/Pending |
ID Technologies, LLC 2020-10-06 |
ARCHON 87910555 not registered Dead/Abandoned |
Eterovich Justin 2018-05-07 |
ARCHON 87460743 5414584 Live/Registered |
Donald Sprouse 2017-05-23 |
ARCHON 86267638 4655972 Live/Registered |
Paul Reed Smith Guitars, Limited Partnership 2014-04-30 |
ARCHON 86243277 not registered Dead/Abandoned |
Batson Enterprises, Inc. 2014-04-04 |
ARCHON 86191770 4890031 Live/Registered |
St. Louis Science Fiction, Ltd. 2014-02-12 |
ARCHON 86191766 4829737 Live/Registered |
St. Louis Science Fiction, Ltd. 2014-02-12 |
ARCHON 85781869 4463893 Live/Registered |
NuVasive, Inc. 2012-11-16 |
ARCHON 85527490 4771057 Live/Registered |
Archon Systems Inc. 2012-01-27 |
ARCHON 85343676 not registered Dead/Abandoned |
Archon Resources, LLC 2011-06-10 |