DRI-LOK 3910-075-802

GUDID 37613327055741

[Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged]

STRYKER CORPORATION

Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use Arthroscopic access cannula, single-use
Primary Device ID37613327055741
NIH Device Record Key7b04d8eb-4f33-4215-8df7-702e93823579
Commercial Distribution StatusIn Commercial Distribution
Brand NameDRI-LOK
Version Model Number3910075802
Catalog Number3910-075-802
Company DUNS187502109
Company NameSTRYKER CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx

Device Dimensions

Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter
Outer Diameter8 Millimeter
Length75 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327055740 [Primary]
GS137613327055741 [Package]
Contains: 07613327055740
Package: pack [5 Units]
In Commercial Distribution

FDA Product Code

NBHAccessories, arthroscopic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-18
Device Publish Date2020-08-10

On-Brand Devices [DRI-LOK]

07613327416558Switching Stick, Large
07613327416541Switching Stick, Small
07613327061123Cannulated Obturator Assembly for Use with 8.0 mm x 75 mm Dri-Lok Cannula Obturator
07613327061116Cannulated Obturator Assembly for Use with 6.5 mm x 75 mm Dri-Lok Cannula Obturator
07613327061109Cannulated Obturator Assembly for Use with 8.0 mm x 90 mm Dri-Lok Cannula Obturator
07613327061093Cannulated 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]

Trademark Results [DRI-LOK]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DRI-LOK
DRI-LOK
78405293 2997454 Live/Registered
Stryker Corporation
2004-04-20
DRI-LOK
DRI-LOK
73298039 1195121 Dead/Cancelled
Litton Systems, Inc.
1981-02-20
DRI-LOK
DRI-LOK
73152094 1115283 Dead/Cancelled
PENN-PLAX PLASTICS, INC.
1977-12-14
DRI-LOK
DRI-LOK
72283250 0870556 Live/Registered
GREEN & GREEN, INC.
1967-10-24

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