Primary Device ID | 03663136027258 |
NIH Device Record Key | 9bda7b2e-1d26-43eb-8227-86372d85fae7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UNI-THREAD® |
Version Model Number | L2ASPL005 |
Company DUNS | 390377518 |
Company Name | SPINEVISION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |
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 | 03663136027258 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03663136027258]
Moist Heat or Steam Sterilization
[03663136027258]
Moist Heat or Steam Sterilization
[03663136027258]
Moist Heat or Steam Sterilization
[03663136027258]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-12-19 |
Device Publish Date | 2015-10-21 |
03663136027258 | Upper Arm |
03663136027135 | BLADE HOLDER 2 |
03663136020044 | Ti 6.5mm x 120mm Right Reduction Rod Connector |
03663136020006 | Ti 6.5mm x 60mm Right Reduction Rod Connector |
03663136006222 | Ti 5.5 mm x 33-38mm threaded reduction screw,6.5mm top |
03663136005867 | Ti 6.5mm x 40mm Right Rod Connector |
03663136005584 | Ti 6.0 mm x 80 mm pre-bent rod |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
UNI-THREAD 78297801 3065015 Live/Registered |
Spinevision S.A. 2003-09-09 |