MicroLink ASB-DGP

GUDID 10845854902080

MicroLink™ CMC Drill Guide with Paddle

Conmed Corporation

Orthopaedic implantation sleeve, reusable

• Primary Device ID: 10845854902080
• NIH Device Record Key: 8081135f-6b45-4d56-bb1a-cf15967ba627
• Commercial Distribution Discontinuation: 2020-08-26
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MicroLink
• Version Model Number: ASB-DGP
• Catalog Number: ASB-DGP
• Company DUNS: 071595540
• Company Name: Conmed 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10845854902080 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

[10845854902080]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-08-28
• Device Publish Date: 2019-07-17

On-Brand Devices [MicroLink]

• 10845854901335: MicroLink™ CMC Trapezium Pin
• 20845854600013: MicroLink™ CMC Trapezium Pin
• 10845854902080: MicroLink™ CMC Drill Guide with Paddle
• 10845854902073: MicroLink™ CMC Drill Guide
• 30845854648531: MICROLINK, CMC DRILL GUIDE WITH PADDLE
• 30845854648524: MICROLINK, CMC DRILL GUIDE
• 30845854648906: MICROLINK, ALL-SUTURE BUTTON AND BACKSTOP (RADIOPAQUE)
• 30845854648890: MICROLINK, ALL-SUTURE BUTTON FIXATION SYSTEM (RADIOPAQUE)
• 30845854648883: MICROLINK, CMC PASSING DRILL
• 30845854648876: MICROLINK, ALL-SUTURE BUTTON FIXATION SYSTEM (RADIOLUCENT)
• 30845854648869: MICROLINK, ALL-SUTURE BUTTON AND BACKSTOP (RADIOLUCENT)
• 10845854901823: MicroLink™ McGlamry Elevator
• 30845854049017: MicroLink™ McGlamry Elevator
• 40845854648903: MICROLINK, ALL-SUTURE BUTTON AND BACKSTOP (RADIOPAQUE)
• 40845854648897: MICROLINK, ALL-SUTURE BUTTON FIXATION SYSTEM (RADIOPAQUE)
• 40845854648873: MICROLINK, ALL-SUTURE BUTTON FIXATION SYSTEM (RADIOLUCENT)
• 40845854648866: MICROLINK, ALL-SUTURE BUTTON AND BACKSTOP (RADIOLUCENT)