CorPath 200 Articulated Arm 160-00807

GUDID 00816280022027

CORINDUS, INC.

Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation Cardiac mapping system workstation

• Primary Device ID: 00816280022027
• NIH Device Record Key: a72e03b1-10fc-43a1-bd16-78b745b12438
• Commercial Distribution Discontinuation: 2019-09-06
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CorPath 200 Articulated Arm
• Version Model Number: 160-00807
• Catalog Number: 160-00807
• Company DUNS: 781746586
• Company Name: CORINDUS, INC.
• 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: false
• Lot Batch: false
• Serial Number: true
• 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: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com
• Phone: 508-653-3335
• Email: customer.service@corindus.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816280022027 [Primary]

FDA Product Code

• DXX: System, Catheter Control, Steerable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-09-11
• Device Publish Date: 2016-09-24

Devices Manufactured by CORINDUS, INC.

• 00816280023185 - CorPath GRX Cassette Duo: 2022-08-16
• 00816280022010 - CorPath 200 Control Console: 2019-09-11
• 00816280022027 - CorPath 200 Articulated Arm: 2019-09-11
• 00816280022027 - CorPath 200 Articulated Arm: 2019-09-11
• 00816280022034 - CorPath 200 Robotic Drive: 2019-09-11
• 00816280022041 - CorPath 200 Cassette: 2019-09-11
• 00816280022072 - CorPath 200 POGO Pin Caps: 2019-09-11
• 00816280022096 - CorPath 200 Control Console Drape: 2019-09-11
• 00816280022119 - CorPath 200 Joystick Covers: 2019-09-11