Archon
GUDID 00887517517074
Beta Archon ACP
Nuvasive, Inc.
Sterilization/disinfection container Sterilization/disinfection container Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable| Primary Device ID | 00887517517074 |
| NIH Device Record Key | b0337e09-fa47-4c1e-8b04-d073b271fea2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Archon |
| Version Model Number | BETARCHON |
| 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 |
Customer Support Contacts
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517517074 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K143579
FDA Product Code
| KCT | Sterilization wrap containers, trays, cassettes & other accessories |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
[00887517517074]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-09-10 |
| Device Publish Date | 2016-09-23 |
On-Brand Devices [Archon]
| 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 |
Trademark Results [Archon]
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 |
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