BIOSCREW C8016

GUDID 20845854034085

BIOSCREW GUIDE WIRES, 356MM (14 IN), QTY 5

Conmed Corporation

Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable
Primary Device ID20845854034085
NIH Device Record Key5838bde4-1c75-48d8-8e8f-9a7357100752
Commercial Distribution StatusIn Commercial Distribution
Brand NameBIOSCREW
Version Model NumberC8016
Catalog NumberC8016
Company DUNS071595540
Company NameConmed Corporation
Device Count5
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM

Device Dimensions

Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter
Length256 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100845854034081 [Unit of Use]
GS110845854034088 [Package]
Contains: 30845854034082
Package: BOX [5 Units]
In Commercial Distribution
GS120845854034085 [Direct Marking]
GS130845854034082 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


[20845854034085]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-02
Device Publish Date2020-09-24

On-Brand Devices [BIOSCREW]

20845854014476BIOSCREW 8MM X 20MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854014452BIOSCREW 9MM X 30MM BIOABSORBABLE INTERFERENCE SCREW
20845854014445BIOSCREW 7MM X 25MM BIOABSORBABLE INTERFERENCE SCREW
20845854014407BIOSCREW 8MM X 25MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854014391BIOSCREW 8MM X 25MM BIOABSORBABLE INTERFERENCE SCREW
20845854014360BIOSCREW 7MM X 25MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854014346BIOSCREW 11MM X 25MM, BIOABSORBABLE INTERFERENCE SCREW
20845854014339BIOSCREW 9MM X 20MM BIOABSORBABLE INTERFERENCE SCREW
20845854014131BIOSCREW 9MM X 25MM BIOABSORBABLE INTERFERENCE SCREW
20845854014049BIOSCREW 7MM X 30MM BIOABSORBABLE INTERFERENCE SCREW
20845854014001BIOSCREW 7MM X 20MM BIOABSORBABLE INTERFERENCE SCREW
20845854013752BIOSCREW 8MM X 30MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854013745BIOSCREW 7MM X 30MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854013738BIOSCREW 9MM X 30MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854013721BIOSCREW 9MM X 20MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854013684BIOSCREW 8MM X 20MM BIOABSORBABLE INTERFERENCE SCREW
20845854013622BIOSCREW 10MM X 30MM BIOABSORBABLE INTERFERENCE SCREW
20845854013615BIOSCREW 11MM X 30MM BIOABSORBABLE INTERFERENCE SCREW
20845854013608BIOSCREW 10MM X 25MM BIOABSORBABLE INTERFERENCE SCREW
20845854013592BIOSCREW 8MM X 30MM BIOABSORBABLE INTERFERENCE SCREW
20845854013561BIOSCREW 7MM X 20MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854013479BIOSCREW 9MM X 25MM BIOABSORBABLE FEMORAL INTERFERENCE SCREW
20845854016678BIOSCREW HYPERFLEX GUIDEWIRES, 356MM (14 IN.), QTY 5
20845854034337BIOSCREW UNIVERSAL TRI-LOBE MODULAR DRIVER
20845854026769BIOSCREW FLEXIBLE DRIVER
20845854016661BIOSCREW UNIVERSAL TRI-LOBE DRIVER
20845854034085BIOSCREW GUIDE WIRES, 356MM (14 IN), QTY 5
20845854041700BioScrew Guidewire, SST, 14in, Sterile
30845854013605BIOSCREW 10MM X 25MM BIOABSORBABLE INTERFERENCE SCREW
00845854034081BIOSCREW GUIDE WIRES, 356MM (14 IN)
00845854016674BIOSCREW HYPERFLEX GUIDEWIRES, 356MM (14 IN.)

Trademark Results [BIOSCREW]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BIOSCREW
BIOSCREW
86673937 4954423 Live/Registered
Conmed Corporation
2015-06-25
BIOSCREW
BIOSCREW
74105000 1724608 Dead/Cancelled
LINVATEC CORPORATION
1990-10-11

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