NUMATRIX 901201

GUDID 10845854080658

CONMED MIXING AND DELIVERY KIT

Conmed Corporation

Arthroscopic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 10845854080658
• NIH Device Record Key: 5b7a0064-d852-43f7-bb07-8f85a9a9f8a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NUMATRIX
• Version Model Number: 901201
• Catalog Number: 901201
• 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: 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

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	10845854080658 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142535

FDA Product Code

• FMF: Syringe, piston

Sterilization

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

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

[10845854080658]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-06-19
• Device Publish Date: 2016-09-24

Devices Manufactured by Conmed Corporation

• 10653405000686 - NA: 2024-07-25 Suction Connecting Tubing, 1.5 Foot (0.46m) 3/16 Inch (4.8mm) ID
• 10845854043691 - CONMED: 2024-07-25 UHD EXTENDED LENGTH AUTOCLAVABLE EYECUP LAPAROSCOPE, 10MM, 30 DEG
• 20845854050320 - CONMED: 2024-07-25 TENDON STRIPPER, OPEN LOOP, DIAM. 6.5 MM
• 50653405000059 - FRAZIER: 2024-07-25 FRAZIER Surgical Suction Instrument, 3Fr with Control Vent and Obturator (Bend with Obturator in Place)
• 10653405000068 - FRAZIER: 2024-07-25 FRAZIER Surgical Suction Instrument, 5Fr with Control Vent and Obturator (Bend with Obturator in Place)
• 10653405000075 - FRAZIER: 2024-07-25 FRAZIER Surgical Suction Instrument, 7Fr with Control Vent and Obturator (Bend with Obturator in Place)
• 10653405000112 - FRAZIER: 2024-07-25 FRAZIER Surgical Suction Instrument, 8Fr with Control Vent and Obturator (Bend with Obturator in Place)
• 50653405000127 - FRAZIER: 2024-07-25 FRAZIER Surgical Suction Instrument, 10Fr with Control Vent and Obturator (Bend with Obturator in Place)