Streamline® Surgical System 10-0066

GUDID 00892064002072

Streamline

NEW WORLD MEDICAL, INCORPORATED

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use

• Primary Device ID: 00892064002072
• NIH Device Record Key: 6f32f56e-c962-47de-a06e-808462e9a900
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Streamline® Surgical System
• Version Model Number: 10-0066 Rev B
• Catalog Number: 10-0066
• Company DUNS: 622768711
• Company Name: NEW WORLD MEDICAL, INCORPORATED
• Device Count: 1
• DM Exempt: true
• 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: true
• Manufacturing Date: true
• 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(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com
• Phone: +1(909)466-4304
• Email: info@newworldmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00892064002072 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K211680

FDA Product Code

• MRH: Pump, infusion, ophthalmic

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: 2023-11-09
• Device Publish Date: 2023-11-01

On-Brand Devices [Streamline® Surgical System]

• 00892064002010: Streamline
• 00892064002072: Streamline