Primary Device ID | 00816818020556 |
NIH Device Record Key | 617f64da-9988-4c10-8d1e-f6119de137ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LinkStation MINI Evaluation Kit |
Version Model Number | LinkStation MINI Evaluation Kit |
Catalog Number | 05000-506 |
Company DUNS | 005788130 |
Company Name | ORTHOSENSOR 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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816818020556 [Primary] |
ONN | Intraoperative Orthopedic Joint Assessment Aid |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-02-20 |
00816818020563 | LinkStation MINI Evaluation Kit with Continental Europe/ Korea power cord and additional label f |
00816818020556 | LinkStation MINI Evaluation Kit with Switzerland power cord |
00816818020549 | LinkStation MINI Evaluation Kit with Italy power cord |
00816818020532 | LinkStation MINI Evaluation Kit with United Kingdom and Ireland power cord |
00816818020525 | LinkStation MINI Evaluation Kit with Continental Europe power cord |
00816818020518 | LinkStation MINI Evaluation Kit with Australia and New Zealand power cord |
00816818020501 | LinkStation MINI Evaluation Kit with power cord for United States and Canada |
00816818022635 | LinkStation MINI Evaluation Kit with power cord for United States and Canada. Bluetooth only. |