Minimed Mio

GUDID 05705244020382

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: 05705244020382
• NIH Device Record Key: 481a3679-d307-4eea-9086-24621a3e4202
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Minimed Mio
• Version Model Number: MMT-965A600
• 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: 1-800-646-4633
• Email: xx@xx.xx

Device Dimensions

• Angle: 90 degree

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store infusion sets in a cool, dry place. Do not leave infusion sets in direct sunlight or inside a vehicle.

Device Identifiers

Device Issuing Agency	Device ID
GS1	05705244020375 [Unit of Use]
GS1	05705244020382 [Package]; Contains: 05705244020399; Package: Outer box [100 Units]; In Commercial Distribution
GS1	05705244020399 [Primary]

FDA Product Code

• FPA: Set, Administration, Intravascular

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-07-19
• Device Publish Date: 2019-07-11

On-Brand Devices [Minimed Mio]

• 05705244020412: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020382: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020351: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020320: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020290: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020269: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020238: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020207: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020115: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244020085: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244025127: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
• 05705244025097: Single use infusion set for subcutaneous infusion. The infusion set must be used as described in