219971

GUDID 10886705021789

Guide Wire Cap

DEPUY MITEK, LLC

Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable

• Primary Device ID: 10886705021789
• NIH Device Record Key: 32a056f0-b3d0-427f-9cd4-24cf1f60d0aa
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 219971
• Catalog Number: 219971
• Company DUNS: 190572854
• Company Name: DEPUY MITEK, LLC
• 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: false
• 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886705021789 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

[10886705021789]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-09-18
• Device Publish Date: 2015-09-01

Devices Manufactured by DEPUY MITEK, LLC

• 10886705010905 - TARGET: 2024-04-03 TARGET TENDON HARVESTER INSTRUMENT
• 10886705010912 - TARGET: 2024-04-03 TARGET DISPOSABLE CUTTING TIPS
• 10886705020591 - FMS VUE: 2024-03-25 FMS VUE Fluid Management System
• 10886705013616 - INTRAFIX: 2023-11-02 FEMORAL INTRAFIX, HARD Includes (1) 7mm Sheath and (1) 6mm Screw 7mm-7.5mm x 23mm
• 10886705013623 - INTRAFIX: 2023-11-02 FEMORAL INTRAFIX, STANDARD Includes (1) 7mm Sheath and (1) 7mm Screw 7mm-7.5mm x 23mm
• 10886705013630 - INTRAFIX: 2023-11-02 FEMORAL INTRAFIX, HARD Includes (1) 8mm Sheath and (1) 7mm Screw 8mm-8.5mm x 23mm
• 10886705013647 - INTRAFIX: 2023-11-02 FEMORAL INTRAFIX, STANDARD Includes (1) 8mm Sheath and (1) 8mm Screw 8mm-8.5mm x 23mm
• 10886705013654 - INTRAFIX: 2023-11-02 FEMORAL INTRAFIX, HARD Includes (1) 9mm Sheath and (1) 8mm Screw 9mm-10mm x 23mm