PARADIGM P1801W

GUDID 20845854650292

PARADIGM ALL-SUTURE ANCHOR 1.8MM, WHITE/BLACK #2

Conmed Corporation

Electrical-only medical device connection cable, reusable

• Primary Device ID: 20845854650292
• NIH Device Record Key: 6fbab08a-3b19-4f11-972d-933e7ea55cc0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PARADIGM
• Version Model Number: P1801W
• Catalog Number: P1801W
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	20845854650292 [Primary]
GS1	20845854901585 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190333

FDA Product Code

• MBI: Fastener, fixation, nondegradable, soft tissue

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-19
• Device Publish Date: 2023-10-11

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• 20845854901417: Paradigm Slim Raven Suture Passer, 15 deg Up
• 30845854082328: Paradigm™Curved Knot Pusher
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• 20653405986819: Paradigm™ ClickLok™ Drill Guide, Straight Fish Mouth
• 20653405986802: Paradigm™ ClickLok™ Drill Guide, Straight Crown
• 20653405986796: Paradigm™ ClickLok™ Drill Guide Obturator
• 20653405986789: Paradigm™ ClickLok™ Drill Bit, 2.1mm
• 20653405986772: Paradigm™ ClickLok™ Anchor, Black #2 Suture
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• 20845854902575: Paradigm, Retractable Blade, Hook
• 20845854902568: Paradigm Retractable Blade, Straight
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• 10845854083048: Paradigm Revolution Medium Boot, Pair
• 10845854083024: Paradigm Revolution Large Boot, Pair
• 10845854083017: Paradigm Revolution Small Boot, Pair
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• 10845854082973: Paradigm Revolution Hip Distractor, EU
• 10845854082966: Paradigm Revolution Hip Distractor, US
• 20845854082932: Paradigm Revolution Perineal Post Pad - Dual Density
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• 30845854082915: Paradigm Boot Disposable Liner, Medium Pair
• 30845854082908: Paradigm Boot Disposable Liner, Small Pair
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• 10845854082959: Paradigm Revolution Left Leg Boom
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