Veriflow™ R-10003

GUDID 00859273007038

Fluid management accessory disposable

RELIGN CORPORATION

Surgical irrigation/aspiration tubing set

• Primary Device ID: 00859273007038
• NIH Device Record Key: b7250ec4-c5b5-45b6-87d2-cb85da799b0a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Veriflow™
• Version Model Number: R-10003
• Catalog Number: R-10003
• Company DUNS: 080031617
• Company Name: RELIGN CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com
• Phone: (866) 608-0131
• Email: customer.service@religncorp.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00859273007038 [Primary]
GS1	08592730070030 [Previous]
GS1	10859273007035 [Package]; Package: Shipper [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162770

FDA Product Code

• HRX: Arthroscope

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: 2020-02-28
• Device Publish Date: 2020-02-20

On-Brand Devices [Veriflow™]

• 08592730070030: Fluid management accessory disposable
• 00859273007038: Fluid management accessory disposable