Primary Device ID | 33760253800564 |
NIH Device Record Key | a8321dd0-b5b1-4ab8-9df1-90ba5f9efa2f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SpineJack |
Version Model Number | 0909300400 |
Catalog Number | 0909-300-400 |
Company DUNS | 196548481 |
Company Name | STRYKER CORPORATION |
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 | 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 |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +0018002533210 |
Inst.Stryker.cs@Stryker.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760253800563 [Primary] |
GS1 | 33760253800564 [Package] Contains: 03760253800563 Package: pack [6 Units] In Commercial Distribution |
KIH | DISPENSER, CEMENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-04 |
Device Publish Date | 2020-07-27 |
33760253800564 | CEMENT PUSHER 4.2MM |
33760253800557 | CEMENT PUSHER 5.0-5.8MM |
33760253800540 | INJECTOR TRANSFER TUBE 4.2MM |
33760253800533 | INJECTOR TRANSFER TUBE 5.0-5.8MM |
03760253800525 | PREPARATION KIT 5.8MM |
03760253800518 | PREPARATION KIT 4.2MM |
03760253800501 | PREPARATION KIT 5.0MM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SPINEJACK 77148228 3539345 Live/Registered |
Vexim, SAS 2007-04-04 |