AEM® Disposable Curved Scissors ES0102

GUDID 10815288010613

ENCISION, INC.

Endoscopic electrosurgical electrode, monopolar, single-use

• Primary Device ID: 10815288010613
• NIH Device Record Key: 88ddbcd9-a808-4c37-af16-06553a5b6133
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AEM® Disposable Curved Scissors
• Version Model Number: ES0102
• Catalog Number: ES0102
• Company DUNS: 612250175
• Company Name: ENCISION, INC.
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 35 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10815288010613 [Primary]
GS1	20815288010610 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191612

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-03-25
• Device Publish Date: 2016-08-31

On-Brand Devices [AEM® Disposable Curved Scissors]

• 10815288010620: ES0102-45
• 10815288010613: ES0102
• 10815288010606: ES0101-45
• 10815288010590: ES0101