Primary Device ID | 07613252495123 |
NIH Device Record Key | a2471c1c-d298-42ea-abb2-182d1090cf72 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SONICFUSION |
Version Model Number | 1910-2212S |
Catalog Number | 1910-2212S |
Company DUNS | 330211587 |
Company Name | Stryker Trauma GmbH |
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 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Size Text, specify | 0 |
Length | 22 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613252495123 [Primary] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-04-15 |
Device Publish Date | 2020-04-07 |
07613327129649 | Instrument Tray |
07613327096071 | TipTool |
07613327096033 | TipTool |
07613327096019 | Handpiece |
07613327095470 | Handpiece Tip |
07613327095463 | Handpiece Tip |
07613327095418 | Drill |
07613327095371 | Drill |
07613252495116 | Instrument Tray SonicPin |
07613252495093 | Foot Switch |
07613252495086 | Handpiece SonicPin |
07613252495079 | Ultrasonic Generator |
07613252495161 | Direct Depth Gauge SonicPin |
07613252495154 | Drill cannulated SonicPin (Pin26mm) |
07613252495147 | Drill SonicPin |
07613252495123 | Drill cannulated SonicPin |
07613252212348 | Drill SonicPin |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SONICFUSION 90124581 not registered Live/Pending |
Oliden Technology, LLC 2020-08-19 |
![]() SONICFUSION 87322006 5353759 Live/Registered |
Stryker European Holdings I, LLC 2017-02-02 |
![]() SONICFUSION 85825919 4395595 Live/Registered |
STRYKER TRAUMA AG 2013-01-17 |
![]() SONICFUSION 78755153 not registered Dead/Abandoned |
STRYKER TRAUMA AG 2005-11-16 |
![]() SONICFUSION 78659021 not registered Dead/Abandoned |
STRYKER TRAUMA AG 2005-06-27 |
![]() SONICFUSION 77750109 4292603 Dead/Cancelled |
STRYKER TRAUMA AG 2009-06-02 |
![]() SONICFUSION 77534831 not registered Dead/Abandoned |
StyleMark, Inc. 2008-07-30 |
![]() SONICFUSION 77534798 not registered Dead/Abandoned |
StyleMark, Inc. 2008-07-30 |