Large applicator

GUDID B108899APC1ENUS0110

BTL INDUSTRIES LIMITED

Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system Multi-modality hyperthermia system

• Primary Device ID: B108899APC1ENUS0110
• NIH Device Record Key: 79e2d23c-6b18-468c-be95-a4b8e5e11937
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Large applicator
• Version Model Number: 899-AP-C-1
• Company DUNS: 733532951
• Company Name: BTL INDUSTRIES LIMITED
• 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: 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
HIBCC	B108899APC1ENUS0110 [Primary]

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: 2021-03-16
• Device Publish Date: 2021-03-08

On-Brand Devices [Large applicator]

• B108899APC1ENUS0100: 899-AP-C-1
• B108899APC1ENUS0110: 899-AP-C-1
• B108899APC1ENUS0120: 899-AP-C-1
• B108785APLMUS00: LARGE applicator
• B108899APC1ENUS0130: 899-AP-C-1
• B108899APC1ENUS0140: 899-AP-C-1