Thermi Disposable RF Electrode (Qty 5) RFDE-VA-EU

GUDID 00817771028993

Thermi Disposable RF Electrode - Qty 5

Celling Biosciences

Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active Medium-wave diathermy treatment system electrode, active

• Primary Device ID: 00817771028993
• NIH Device Record Key: 2f782e69-674b-47a4-b259-bafd7ed058f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Thermi Disposable RF Electrode (Qty 5)
• Version Model Number: RFDE-VA-EU (Qty5)
• Catalog Number: RFDE-VA-EU
• Company DUNS: 021560394
• Company Name: Celling Biosciences
• 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: true
• Expiration Date: true
• 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	00817771028993 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173582

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-25
• Device Publish Date: 2023-09-17

On-Brand Devices [Thermi Disposable RF Electrode (Qty 5)]

• 00817771029129: Thermi Disposable RF Electrode - 20W Qty 5
• 00817771029105: Thermi Disposable RF Electrode - Qty 5
• 00817771029037: Thermi Disposable RF Electrode - Qty 5
• 00817771028993: Thermi Disposable RF Electrode - Qty 5
• 00817771028979: Thermi Disposable RF Electrode - 50W Qty 5