HYPERFLEX 8572D

GUDID 20845854041625

HYPERFLEX GUIDEWIRE, NITINOL, 14IN, STERILE

Conmed Corporation

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• Primary Device ID: 20845854041625
• NIH Device Record Key: eca4c543-5fc0-453b-8715-d042ad91894a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HYPERFLEX
• Version Model Number: 8572D
• Catalog Number: 8572D
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 5
• 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

Customer Support Contacts

• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Device Dimensions

• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch
• Length: 14 Inch

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing Agency	Device ID
GS1	00845854041621 [Unit of Use]
GS1	10845854041628 [Primary]
GS1	20845854041625 [Package]; Contains: 10845854041628; Package: CARTON [5 Units]; In Commercial Distribution

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

[20845854041625]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-12-21
• Device Publish Date: 2020-12-13

On-Brand Devices [HYPERFLEX]

• 20845854041618: HYPERFLEX GUIDEWIRE, NITINOL, 9 IN, STERILE, 1.6 X 229MM (.062 X 9IN)
• 20845854041632: HYPERFLEX GUIDEWIRE, NITINOL, 18.5IN, STERILE
• 20845854041625: HYPERFLEX GUIDEWIRE, NITINOL, 14IN, STERILE
• 00845854025331: 1.6 X 356MM (.062IN X 14IN) HYPERFLEX FLEXIBLE GUIDE WIRE
• 00845854025317: 1.6 X 229MM (.062 IN X 9IN) HYPERFLEX NITINOL GUIDE WIRE