Primary Device ID | 07613327368505 |
NIH Device Record Key | d9b49138-df83-4b13-bde6-b71ec4b57433 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | T2 ALPHA |
Version Model Number | 2360-5110S |
Catalog Number | 2360-5110S |
Company DUNS | 330211587 |
Company Name | Stryker Trauma GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Size Text, specify | 0 |
Length | 110 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327368505 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-11-29 |
Device Publish Date | 2018-10-29 |
07613327411881 | Opening 13mm Insert |
07613327411874 | Femur Antegrade GT Indication Tray Base |
07613327411867 | Opening 11.5mm Insert |
07613327411836 | Basic Tray Base |
07613327411812 | Femur Antegrade PF Indication Tray Base |
07613327411737 | Femur Antegrade GT/PF Indication Insert |
07613327411720 | Upgrade Instruments Insert |
07613327411713 | Femur Antegrade Distal Targeting Tray |
07613327411706 | Femur Antegrade PF Indication Tray |
07613327411690 | Basic Tray Insert |
07613327411683 | Tibia Distal Targeting Tray |
07613327411676 | Drills and Pins Insert |
07613327411669 | Basic Tray |
07613327411638 | Femur Antegrade GT Indication Tray |
07613327411621 | SPI Insert |
07613327411553 | Tibia Indication Tray |
07613327368932 | Reamer Head Insert |
07613327368598 | Locking Screw |
07613327368581 | Locking Screw |
07613327368574 | Locking Screw |
07613327368567 | Locking Screw |
07613327368550 | Locking Screw |
07613327368543 | Locking Screw |
07613327368536 | Locking Screw |
07613327368529 | Locking Screw |
07613327368512 | Locking Screw |
07613327368505 | Locking Screw |
07613327368499 | Locking Screw |
07613327368482 | Locking Screw |
07613327368475 | Locking Screw |
07613327368468 | Locking Screw |
07613327368451 | Locking Screw |
07613327366280 | Nail Holding Screw Tibia / Femur PF |
07613327366235 | Locking Screw |
07613327366228 | Locking Screw |
07613327366211 | Locking Screw |
07613327366204 | Locking Screw |
07613327366198 | Locking Screw |
07613327366181 | Locking Screw |
07613327366174 | Locking Screw |
07613327366167 | Locking Screw |
07613327366150 | Locking Screw |
07613327366143 | Locking Screw |
07613327366136 | Locking Screw |
07613327366129 | Locking Screw |
07613327365092 | Compression Screw Tibia |
07613327365078 | End Cap Tibia |
07613327365061 | End Cap Tibia |
07613327365047 | End Cap Tibia |
07613327365030 | End Cap Tibia |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() T2 ALPHA 87221226 not registered Live/Pending |
Stryker European Holdings I, LLC 2016-10-31 |