Dual Infusion Pump Tube Set

GUDID 10627825000441

Laborie Medical Technologies Canada ULC

Electric infusion pump administration set, single-use

• Primary Device ID: 10627825000441
• NIH Device Record Key: 3fe80d02-6ad5-4c63-b0af-22f21d01a14e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dual Infusion Pump Tube Set
• Version Model Number: DIPTS-LT2
• Company DUNS: 203383526
• Company Name: Laborie Medical Technologies Canada ULC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00627825000444 [Primary]
GS1	10627825000441 [Package]; Contains: 00627825000444; Package: [25 Units]; In Commercial Distribution

FDA Product Code

• FEN: DEVICE, CYSTOMETRIC, HYDRAULIC

Sterilization

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

[10627825000441]

Ethylene Oxide

[10627825000441]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-21

On-Brand Devices [Dual Infusion Pump Tube Set]

• 10627825000441: DIPTS-LT2
• 10627825000427: DIPTS-LT1