Minimed Mio

GUDID 05705244020351

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	05705244020351
NIH Device Record Key	db928ffa-c5a6-4ef1-9ce4-766fe91d4361
Commercial Distribution Status	In Commercial Distribution
Brand Name	Minimed Mio
Version Model Number	MMT-945A600
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
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx
Phone	1-800-646-4633
Email	xx@xx.xx

Device Dimensions

Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	80 Centimeter
Depth	6 Millimeter
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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	05705244020344 [Unit of Use]
GS1	05705244020351 [Package] Contains: 05705244020368 Package: Outer box [100 Units] In Commercial Distribution
GS1	05705244020368 [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