Primary Device ID | 00887517102560 |
NIH Device Record Key | ef171b73-f617-482f-99eb-5972ea55c885 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 1552360 |
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 | 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 |
Phone | +1(858)909-1800 |
RA_UDI@nuvasive.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887517102560 [Primary] |
BSK | Cuff, tracheal tube, inflatable |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887517102560]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-23 |
Device Publish Date | 2019-07-15 |
00195377161307 - ReLine | 2024-05-29 RELINE Reducer, Politician |
00195377161314 - ReLine | 2024-05-29 RELINE Lock Screw Starter, Politician |
00195377055521 - Nimbus | 2024-05-01 Maxcess Adapter, A-Arm Threaded |
00195377055538 - Nimbus | 2024-05-01 Nimbus Adapter, Large Clamp |
00195377055545 - Nimbus | 2024-05-01 Nimbus Adapter, Medium Clamp |
00195377055552 - Nimbus | 2024-05-01 Nimbus Adapter, Small Clamp |
00195377061232 - Nimbus | 2024-05-01 Nimbus Adapters Tray |
00195377159847 - XLIF | 2024-05-01 XLIF Prone Anchor and Shim, Fixation Lt |