Veriflow™ R-10003

GUDID 08592730070030

Fluid management accessory disposable

RELIGN CORPORATION

Surgical irrigation/aspiration tubing set

• Primary Device ID: 08592730070030
• NIH Device Record Key: 7ce1314d-2cdf-4436-8511-badede41f88b
• 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.co

Device Identifiers

Device Issuing Agency	Device ID
GS1	08592730070030 [Primary]
GS1	18592730070037 [Package]; Package: Customer Shipper Box [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-04-23
• Device Publish Date: 2018-12-10

On-Brand Devices [Veriflow™]

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