Varisoft

GUDID 05705244018730

Single use infusion set for subcutaneous infusion. The infusion set must be used as described in the Instruction for Use.

Unomedical A/S

Electric infusion pump administration set, single-use

• Primary Device ID: 05705244018730
• NIH Device Record Key: a8b25f06-0b63-4d7c-a520-782fb7bfe7c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Varisoft
• Version Model Number: 1002828
• Company DUNS: 306032491
• Company Name: Unomedical A/S
• Device Count: 10
• 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: 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

Customer Support Contacts

• Phone: 1-858-255-6269
• Email: xx@xx.xx

Device Dimensions

• Angle: 30 degree
• Angle: 30 degree
• Angle: 30 degree

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Protect from direct sunlight and atmospheric humidity. Store in a dry place at room temperature.

Device Identifiers

Device Issuing Agency	Device ID
GS1	05705244018723 [Primary]
GS1	05705244018730 [Package]; Contains: 05705244018723; Package: Outer Box [100 Units]; In Commercial Distribution
GS1	05705244018747 [Unit of Use]

FDA Product Code

• FPA: Set, Administration, Intravascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-03-26
• Device Publish Date: 2019-03-15

On-Brand Devices [Varisoft]

• 05705244018853: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244018792: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244018730: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244018709: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244014855: Single use infusion set for subcutaneous infusion. The infusion set must be used as described
• 05705244014824: Single use infusion set for subcutaneous infusion. The infusion set must be used as described
• 05705244014794: Single use infusion set for subcutaneous infusion. The infusion set must be used as described
• 05705244014763: Single use infusion set for subcutaneous infusion. The infusion set must be used as described
• 05705244014732: Single use infusion set for subcutaneous infusion. The infusion set must be used as described
• 05705244014701: Single use infusion set for subcutaneous infusion. The infusion set must be used as described