neria™ detach

GUDID 05705244000995

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: 05705244000995
• NIH Device Record Key: 7ee9fede-1a28-4963-9400-f09314f4fd64
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: neria™ detach
• Version Model Number: 78-110-2721
• 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: false
• 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

• Length: 110 Centimeter
• Depth: 10 Millimeter
• Angle: 90 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	05705244000995 [Primary]
GS1	05705244001008 [Package]; Package: Outer box [200 Units]; In Commercial Distribution
GS1	05705244010888 [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: 2018-03-29
• Device Publish Date: 2016-09-15

On-Brand Devices [neria™ detach]

• 05705244000995: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244000971: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244000957: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244000933: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244000919: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244000896: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244000872: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244000858: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244000834: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in