Reprocessed OPES Aspirating Ablator, 3mm, 90 deg

GUDID B390AR9703A901

SURETEK MEDICAL

Endoscopic electrosurgical handpiece/electrode, monopolar, reprocessed

• Primary Device ID: B390AR9703A901
• NIH Device Record Key: 5e5178e0-dd95-44e0-a77d-f172089b73b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed OPES Aspirating Ablator, 3mm, 90 deg
• Version Model Number: AR-9703A-90
• Company DUNS: 785616934
• Company Name: SURETEK MEDICAL
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B390AR9703A901 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K052692

FDA Product Code

• NUJ: Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

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: 2018-07-06
• Device Publish Date: 2016-09-02

On-Brand Devices [Reprocessed OPES Aspirating Ablator, 3mm, 90 deg]

• B390AR9803A901: AR-9803A-90
• B390AR9703A901: AR-9703A-90