Bipolar Scissor SBPSC08

GUDID 00810026180538

Bipolar Scissor (Crv.) 7" (18cm), Reusable

SONIQUENCE, LLC

Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

• Primary Device ID: 00810026180538
• NIH Device Record Key: f19a76ae-1768-4a06-a281-6649d71ebe10
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bipolar Scissor
• Version Model Number: SBPSC08
• Catalog Number: SBPSC08
• Company DUNS: 117308190
• Company Name: SONIQUENCE, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	00810026180538 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042608

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

[00810026180538]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-09-27
• Device Publish Date: 2021-09-19

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• 00810026181535 - RF Generator: 2023-04-04 RF Generator
• 00810026181542 - RF Generator: 2023-04-04 RF Generator
• 00810026181559 - RF Generator: 2023-04-04 RF Generator