Instruments
GUDID 00887517381972
ALGI Instruments Base,Sterilization Case
Nuvasive, Inc.
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 Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable| Primary Device ID | 00887517381972 |
| NIH Device Record Key | a49cf49e-2e7d-489e-96b2-991bdf949212 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Instruments |
| Version Model Number | 6900093 |
| 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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517381972 [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 |
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
[00887517381972]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-14 |
| Device Publish Date | 2023-09-06 |
On-Brand Devices [Instruments]
| 00887517387462 | ALGI Rongeur, Large Dismantlable |
| 00887517387455 | ALGI Rongeur, Small Dismantlable |
| 00887517385819 | ALGI Rongeur, Pituitary Medium |
| 00887517385529 | ALGI Rasp, Serrated |
| 00887517385185 | ALGI Curette, Up Angled Small |
| 00887517385147 | ALGI Curette, Straight Medium |
| 00887517385130 | ALGI Curette, Down Facing Large |
| 00887517385123 | ALGI Curette, Down Facing Medium |
| 00887517385116 | ALGI Curette, Down Facing Small |
| 00887517385109 | ALGI Curette, Up Angled Large |
| 00887517384690 | ALGI Curette, Up Angled Medium |
| 00887517384652 | ALGI Curette, Straight Small |
| 00887517384645 | ALGI Curette, Straight Large |
| 00887517384331 | ALGI Cobb Elevator, Down Small |
| 00887517384324 | ALGI Cobb Elevator, Straight Small |
| 00887517384317 | ALGI Cobb Elevator, Down Large |
| 00887517384300 | ALGI Cobb Elevator, Straight Large |
| 00887517383518 | ALGI Disc Cutter, 14mm |
| 00887517383501 | ALGI Disc Cutter, 12mm |
| 00887517383099 | ALGI Disc Cutter, 10mm |
| 00887517383082 | ALGI Disc Cutter, 8mm |
| 00887517382696 | ALGI Chisel, 12mm Straight |
| 00887517382689 | ALGI Chisel, 7mm Straight |
| 00887517199683 | ALGI Bi-Polar, 12.5 Str Bayonetted |
| 00887517070258 | ALGI Suction, 12 FR Long |
| 00887517066497 | ALGI Suction, 10 FR Long |
| 00887517073532 | ALGI Bipolar Cable, Fixed Pins |
| 00887517066466 | ALGI Nerve Retractor, Long |
| 00887517066473 | ALGI Nerve Retractor, Suction Long |
| 00887517382337 | Sterilization Case Base, AGI 2 Instrume |
| 00887517381972 | ALGI Instruments Base,Sterilization Case |
Trademark Results [Instruments]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 INSTRUMENTS 77377334 3551521 Live/Registered |
Apple Inc. 2008-01-22 |
 INSTRUMENTS 76556647 not registered Dead/Abandoned |
Chanel, Inc. 2003-10-17 |
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