S3ESCLS

GUDID 04573596212318

Probe

FUJIFILM HEALTHCARE CORPORATION

Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable Oesophageal ultrasound imaging transducer, reusable

• Primary Device ID: 04573596212318
• NIH Device Record Key: 88a06dd3-e689-4160-880b-cdbcbb0cae64
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: S3ESCLS
• Version Model Number: S3ESCLS
• Company DUNS: 680160734
• Company Name: FUJIFILM HEALTHCARE 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: 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
GS1	04573596212318 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191233

FDA Product Code

• IYN: System, Imaging, Pulsed Doppler, Ultrasonic

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: 2024-02-02
• Device Publish Date: 2024-01-25

Devices Manufactured by FUJIFILM HEALTHCARE CORPORATION

• 04573596212011 - L31KP: 2024-02-02 Probe
• 04573596212318 - S3ESCLS: 2024-02-02Probe
• 04573596212318 - S3ESCLS: 2024-02-02 Probe
• 04573596212035 - L35: 2024-01-30 Probe
• 04573596212455 - UST-2266-5: 2024-01-30 Probe
• 04573596214176 - CL4416R1: 2024-01-30 Probe
• 04573596214336 - C421: 2024-01-30 Probe
• 04573596214503 - CC41R2: 2024-01-30 Probe
• 04573596214510 - C253A: 2024-01-30 Probe