A&E Medical / Disposable Suction Coagulator

GUDID 20841291104879

Suction Coagulator, 50 per box

A & E MEDICAL CORPORATION

Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use

• Primary Device ID: 20841291104879
• NIH Device Record Key: d141dbd5-3035-4ef1-bdd5-454258fd60e1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A&E Medical / Disposable Suction Coagulator
• Version Model Number: 050-006
• Company DUNS: 173770868
• Company Name: A & E MEDICAL CORPORATION
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	20841291104879 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K881413

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

[20841291104879]

Radiation Sterilization

[20841291104879]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-11-29

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• 20841291104879: Suction Coagulator, 50 per box