AEM® Disposable Electrode, L-Diamond FC0311-45

GUDID 20815288012508

ENCISION, INC.

Endoscopic electrosurgical electrode, monopolar, single-use

• Primary Device ID: 20815288012508
• NIH Device Record Key: df00068d-0719-4476-9e2e-c10d203ea1eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AEM® Disposable Electrode, L-Diamond
• Version Model Number: FC0311-45
• Catalog Number: FC0311-45
• 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: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter
• Length: 45 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10815288012501 [Primary]
GS1	20815288012508 [Package]; Contains: 10815288012501; Package: [10 Units]; In Commercial Distribution

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: 2020-10-29
• Device Publish Date: 2016-08-31

On-Brand Devices [AEM® Disposable Electrode, L-Diamond]

• 20815288012508: FC0311-45
• 20815288012492: FC0311