Dual Adhesive Strap

GUDID 10627987360155

1929803 Ontario Corp

Noninvasive vascular ultrasound system probe

• Primary Device ID: 10627987360155
• NIH Device Record Key: 97ac154a-7639-491e-afa5-1ea8b1de626f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dual Adhesive Strap
• Version Model Number: FP120-FOT01-006
• Company DUNS: 204195374
• Company Name: 1929803 Ontario Corp
• 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: 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	00627987360158 [Primary]
GS1	10627987360155 [Package]; Contains: 00627987360158; Package: Bag [10 Units]; In Commercial Distribution

FDA Product Code

• DPW: Flowmeter, Blood, Cardiovascular

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: 2025-07-01
• Device Publish Date: 2025-06-23

On-Brand Devices [Dual Adhesive Strap]

• 10627987360148: FP120-FOT01-005
• 10627987360155: FP120-FOT01-006