Pump Tubing Infusion Line

GUDID 10627825000038

Laborie Medical Technologies Canada ULC

Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use

• Primary Device ID: 10627825000038
• NIH Device Record Key: 286baaf0-75a8-47b0-8991-5d12ef8f7f4e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pump Tubing Infusion Line
• Version Model Number: TUB500
• 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	00627825000031 [Primary]
GS1	10627825000038 [Package]; Contains: 00627825000031; Package: [25 Units]; In Commercial Distribution
GS1	20627825000035 [Package]; Package: [200 Units]; In Commercial Distribution
GS1	30627825000032 [Package]; Contains: 00627825000031; Package: [10 Units]; In Commercial Distribution
GS1	40627825000039 [Package]; Contains: 30627825000032; Package: [20 Units]; In Commercial Distribution

FDA Product Code

• FEN: DEVICE, CYSTOMETRIC, HYDRAULIC

Sterilization

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

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

Ethylene Oxide

[10627825000038]

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

Devices Manufactured by Laborie Medical Technologies Canada ULC

• 30627825007024 - Extension Set 2: 2022-07-04
• 20627825007294 - Extension Line, 60 cm: 2022-07-04
• 20627825007317 - Extension Line, 1500mm: 2022-07-04
• 20627825007324 - Extension Line, 15cm: 2022-07-04
• 20627825007348 - Extension Line, 150cm Blue: 2022-07-04
• 30627825007352 - Extension Line, 150cm Yellow: 2022-07-04
• 20627825007034 - Extension Set 3: 2022-07-04
• 30627825007307 - Extension Line, 90 cm: 2022-07-04