Primary Device ID | 00812258029210 |
NIH Device Record Key | d0628e27-71cd-4514-b182-cd42a5cfead1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PRECICE® Approach Instrument Tray |
Version Model Number | NGI2-000 |
Catalog Number | NGI2-000 |
Company DUNS | 837845234 |
Company Name | NUVASIVE SPECIALIZED ORTHOPEDICS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00812258029210 [Primary] |
HSB | Rod, Fixation, Intramedullary And Accessories |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
[00812258029210]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-08-09 |
Device Publish Date | 2017-10-10 |
00195377168276 - PRECICE Screws | 2024-01-19 5.0 mm X 100 mm Locking Screw, Fully Threaded |
00195377168283 - PRECICE Screws | 2024-01-19 5.0 mm X 95 mm Locking Screw, Fully Threaded |
00195377168290 - PRECICE Screws | 2024-01-19 5.0 mm X 80 mm Locking Screw, Fully Threaded |
00195377168603 - PRECICE Screws | 2024-01-19 5.0 mm X 70 mm Locking Screw, Fully Threaded |
00195377168610 - PRECICE Screws | 2024-01-19 5.0 mm X 60 mm Locking Screw, Fully Threaded |
00195377168627 - PRECICE Screws | 2024-01-19 5.0 mm X 50 mm Locking Screw, Fully Threaded |
00195377168634 - PRECICE Screws | 2024-01-19 5.0 mm X 45 mm Locking Screw, Fully Threaded |
00195377168641 - PRECICE Screws | 2024-01-19 5.0 mm X 32.5 mm Locking Screw, Fully Threaded |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRECICE 97287304 not registered Live/Pending |
PRECICE MOTORSPORTS LLC 2022-02-28 |
PRECICE 88073801 not registered Live/Pending |
Epic Ice, LLC 2018-08-10 |
PRECICE 85064864 4158334 Live/Registered |
NUVASIVE, INC. 2010-06-16 |
PRECICE 76250632 not registered Dead/Abandoned |
KLA-Tencor Corporation 2001-05-03 |
PRECICE 75092861 not registered Dead/Abandoned |
Cadence Design Systems, Inc. 1996-04-23 |
PRECICE 75072688 not registered Dead/Abandoned |
BIODEX MEDICAL SYSTEMS, INC. 1996-03-14 |