RONIN

GUDID 00850061395009

HEADLAMP, OPERATING, BATTERY-OPERATED

Ronin Surgical Corp.

Head-worn lamp

• Primary Device ID: 00850061395009
• NIH Device Record Key: a6a04be3-dca0-4e7f-a506-ef7942d6479e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RONIN
• Version Model Number: X6
• Company DUNS: 059816500
• Company Name: Ronin Surgical Corp.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Manufacturing Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850061395009 [Primary]

FDA Product Code

• HPP: Headlamp, Operating, Battery-Operated

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-31
• Device Publish Date: 2024-05-23