CPS GS1013

GUDID 20845854045340

CPS CONTINUOUS PRESSURE SENSING TUBING SET WITH FILTER

Conmed Corporation

Insufflation gas conditioning tubing set

• Primary Device ID: 20845854045340
• NIH Device Record Key: 47a64190-dcaa-4d1a-87ea-0a8879126da7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CPS
• Version Model Number: GS1013
• Catalog Number: GS1013
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 10
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00845854045346 [Unit of Use]
GS1	10845854045343 [Primary]
GS1	20845854045340 [Package]; Contains: 10845854045343; Package: CARTON [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K983326

FDA Product Code

• HIF: INSUFFLATOR, LAPAROSCOPIC

Sterilization

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

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

[20845854045340]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-11-29
• Device Publish Date: 2016-09-24

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