Primary Device ID | 07613327093308 |
NIH Device Record Key | 6774ea17-07bf-4e72-9554-b4e8a4f1ad43 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 5150-9-960 |
Catalog Number | 5150-9-960 |
Company DUNS | 481999654 |
Company Name | Stryker Trauma SA |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 | 07613327093308 [Primary] |
JDW | PIN, FIXATION, THREADED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |
07613327606010 - REUNION | 2024-08-30 Humeral 1 Express Tray |
07613327606027 - REUNION | 2024-08-30 Humeral 1 Express Insert |
07613327606034 - REUNION | 2024-08-30 Humeral 2 Express Insert |
07613327606041 - REUNION | 2024-08-30 Reverse Express Insert |
07613327606058 - REUNION | 2024-08-30 Anatomic Express Insert |
07613327606065 - REUNION | 2024-08-30 Anatomic Express Tray |
07613327606072 - REUNION | 2024-08-30 Reverse Express Tray |
07613327606089 - REUNION | 2024-08-30 Humeral 2 Express Tray |