Transducer C5-1

GUDID 00884838100213

Introduction of C5-1 (Shanghai Version) to rest of the world.

Philips Ultrasound LLC

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 00884838100213
• NIH Device Record Key: 887c048e-7d51-48fe-b59f-ff4a89585572
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Transducer C5-1
• Version Model Number: 989606714071
• Company DUNS: 063377717
• Company Name: Philips Ultrasound 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: 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	00884838100213 [Primary]

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: 2024-08-07
• Device Publish Date: 2024-07-30

Devices Manufactured by Philips Ultrasound LLC

• 00884838123625 - Ultrasound System 5500CV: 2025-07-28 As part of SW 2.0
• 00884838123632 - Ultrasound System 5500P: 2025-07-28 Part of SW 2.0
• 00884838123649 - Ultrasound System 5500W: 2025-07-28 Part of SW 2.0
• 00884838123656 - Ultrasound System 5300G: 2025-07-28 Part of SW 2.0
• 00884838123663 - Ultrasound System 5300W: 2025-07-28 As part of SW 2.0
• 00884838123670 - Ultrasound System 5300P: 2025-07-28 As part of SW 2.0
• 00884838123687 - Ultrasound System 5500G: 2025-07-28 As part of SW 2.0
• 00884838125964 - Lumify USB-C to USB-C Transducer cable: 2025-07-22 Lumify USB-C to USB-C Transducer cable