NuWav

GUDID 00627825005555

Laborie Medical Technologies Canada ULC

General-purpose ultrasound imaging system

• Primary Device ID: 00627825005555
• NIH Device Record Key: 04ac6c7c-e520-4ae8-96b3-6b515b37106b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NuWav
• Version Model Number: PRB265
• Company DUNS: 203383526
• Company Name: Laborie Medical Technologies Canada ULC
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00627825005555 [Primary]

FDA Product Code

• IYO: System, imaging, pulsed echo, ultrasonic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-05-23
• Device Publish Date: 2016-09-21

On-Brand Devices [NuWav]

• 00627825005562: PRB266
• 00627825005555: PRB265
• 00627825005548: PRB260
• 00627825005531: PRB250
• 00627825005524: PRB240
• 00627825005517: PRB262