Primary Device ID | 37613327055758 |
NIH Device Record Key | 587e21e6-c9ea-456d-bd11-043e497dfa67 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DRI-LOK |
Version Model Number | 3910090500 |
Catalog Number | 3910-090-500 |
Company DUNS | 187502109 |
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 | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx | |
Phone | +1(866)624-4422 |
xx@xx.xx |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 90 Millimeter |
Outer Diameter | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327055757 [Primary] |
GS1 | 37613327055758 [Package] Contains: 07613327055757 Package: pack [5 Units] In Commercial Distribution |
NBH | Accessories, arthroscopic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-18 |
Device Publish Date | 2020-08-10 |
07613327416558 | Switching Stick, Large |
07613327416541 | Switching Stick, Small |
07613327061123 | Cannulated Obturator Assembly for Use with 8.0 mm x 75 mm Dri-Lok Cannula Obturator |
07613327061116 | Cannulated Obturator Assembly for Use with 6.5 mm x 75 mm Dri-Lok Cannula Obturator |
07613327061109 | Cannulated Obturator Assembly for Use with 8.0 mm x 90 mm Dri-Lok Cannula Obturator |
07613327061093 | Cannulated Obturator Assembly for Use with 8.0 mm x 90 mm Dri-Lok Cannula Obturator |
37613327055802 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055796 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055789 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055772 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055765 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055758 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055741 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055734 | [Non-Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055727 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055710 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055703 | [Non-Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055697 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055680 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055673 | [Non-Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
37613327055666 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DRI-LOK 78405293 2997454 Live/Registered |
Stryker Corporation 2004-04-20 |
DRI-LOK 73298039 1195121 Dead/Cancelled |
Litton Systems, Inc. 1981-02-20 |
DRI-LOK 73152094 1115283 Dead/Cancelled |
PENN-PLAX PLASTICS, INC. 1977-12-14 |
DRI-LOK 72283250 0870556 Live/Registered |
GREEN & GREEN, INC. 1967-10-24 |