LEEP PRECISION™ Generator

GUDID 00888937014235

LEEP PRECISION™ Generator (120 VAC)

Coopersurgical, Inc.

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• Primary Device ID: 00888937014235
• NIH Device Record Key: 87288c09-fcaa-4c10-a74c-1be30eea5f20
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LEEP PRECISION™ Generator
• Version Model Number: LP-20-120
• Company DUNS: 801895244
• Company Name: Coopersurgical, 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: false
• Lot Batch: false
• Serial Number: true
• 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	00888937014235 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K963653

FDA Product Code

• HGI: Electrocautery, Gynecologic (And Accessories)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-22

On-Brand Devices [LEEP PRECISION™ Generator]

• 00888937019926: LEEP PRECISION™ Generator (120 VAC)
• 00888937014235: LEEP PRECISION™ Generator (120 VAC)