TruSteel

GUDID 05705244018525

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: 05705244018525
• NIH Device Record Key: 7cb3f513-d51b-4aae-9517-4252df200bc7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TruSteel
• Version Model Number: 1002836
• 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: 90 degree
• Angle: 90 degree
• Angle: 90 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	05705244018518 [Primary]
GS1	05705244018525 [Package]; Contains: 05705244018518; Package: Outer Box [100 Units]; In Commercial Distribution
GS1	05705244018532 [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 [TruSteel]

• 05705244018525: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244018495: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244018464: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244018433: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244014978: Single use infusion set for subcutaneous infusion. The infusion set must be used as described
• 05705244014947: Single use infusion set for subcutaneous infusion. The infusion set must be used as described
• 05705244014916: Single use infusion set for subcutaneous infusion. The infusion set must be used as described
• 05705244014886: Single use infusion set for subcutaneous infusion. The infusion set must be used as described