HYPERFLEX 8573D

GUDID 20845854041632

HYPERFLEX GUIDEWIRE, NITINOL, 18.5IN, STERILE

Conmed Corporation

Surgical drill guide, single-use
Primary Device ID20845854041632
NIH Device Record Key051b867e-573b-47e9-a20a-0fe5a8214568
Commercial Distribution StatusIn Commercial Distribution
Brand NameHYPERFLEX
Version Model Number8573D
Catalog Number8573D
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 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)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com

Device Dimensions

Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch
Length18.5 Inch

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing AgencyDevice ID
GS100845854041638 [Unit of Use]
GS110845854041635 [Primary]
GS120845854041632 [Package]
Contains: 10845854041635
Package: CARTON [5 Units]
In Commercial Distribution

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

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[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


[20845854041632]

Radiation Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-21
Device Publish Date2020-12-13

On-Brand Devices [HYPERFLEX]

20845854041618HYPERFLEX GUIDEWIRE, NITINOL, 9 IN, STERILE, 1.6 X 229MM (.062 X 9IN)
20845854041632HYPERFLEX GUIDEWIRE, NITINOL, 18.5IN, STERILE
20845854041625HYPERFLEX GUIDEWIRE, NITINOL, 14IN, STERILE
008458540253311.6 X 356MM (.062IN X 14IN) HYPERFLEX FLEXIBLE GUIDE WIRE
008458540253171.6 X 229MM (.062 IN X 9IN) HYPERFLEX NITINOL GUIDE WIRE

Trademark Results [HYPERFLEX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HYPERFLEX
HYPERFLEX
98301664 not registered Live/Pending
FootBridge Medical LLC
2023-12-06
HYPERFLEX
HYPERFLEX
98200295 not registered Live/Pending
Shanghai MicroPort Endovascular MedTech(Group) Co., Ltd.
2023-09-27
HYPERFLEX
HYPERFLEX
97935472 not registered Live/Pending
Schmitz, Gregory P.
2023-05-14
HYPERFLEX
HYPERFLEX
97289206 not registered Live/Pending
Legend Valve & Fitting, Inc
2022-03-01
HYPERFLEX
HYPERFLEX
90253905 not registered Live/Pending
Pipeline Induction Heat Ltd
2020-10-14
HYPERFLEX
HYPERFLEX
88312318 not registered Live/Pending
Legend Valve & Fitting, Inc
2019-02-22
HYPERFLEX
HYPERFLEX
88176738 not registered Live/Pending
TruFlex Sanders, LLC
2018-10-31
HYPERFLEX
HYPERFLEX
87652553 5760359 Live/Registered
Floorguard Products, Inc.
2017-10-19
HYPERFLEX
HYPERFLEX
87173649 not registered Dead/Abandoned
MSC Gaming, Inc.
2016-09-16
HYPERFLEX
HYPERFLEX
87118875 not registered Live/Pending
Cisco Technology, Inc.
2016-07-27
HYPERFLEX
HYPERFLEX
86250421 4905693 Live/Registered
Altera Corporation
2014-04-11
HYPERFLEX
HYPERFLEX
85889721 not registered Dead/Abandoned
Supply House Industrial Products, Inc.
2013-03-28

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