neria™soft cannula

GUDID 05705244001091

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

Unomedical A/S

Electric infusion pump administration set, single-use

• Primary Device ID: 05705244001091
• NIH Device Record Key: 96775ac6-b93b-4faf-908c-553c4f272736
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: neria™soft cannula
• Version Model Number: 76-000-2552
• 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

Device Dimensions

• Angle: 30 degree
• Angle: 30 degree

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Protect from direct sunlight. Store at room temperature.

Device Identifiers

Device Issuing Agency	Device ID
GS1	05705244001091 [Primary]
GS1	05705244001107 [Package]; Package: Outer box [200 Units]; In Commercial Distribution
GS1	05705244010475 [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: 3
• Public Version Date: 2020-03-12
• Device Publish Date: 2016-09-15

On-Brand Devices [neria™soft cannula]

• 05705244001534: Single use infusion cannula for subcutaneous infusion. The infusion cannula must be used as desc
• 05705244001091: Single use infusion cannula for subcutaneous infusion. The infusion cannula must be used as desc