Primary Device ID | 05705244019904 |
NIH Device Record Key | fbaebcaa-962b-4d1e-8713-63a4bc2712ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Minimed™ Mio™ |
Version Model Number | MMT-921A |
Catalog Number | NA |
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 |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
Angle | 90 degree |
Depth | 6 Millimeter |
Length | 46 Centimeter |
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 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 05705244019898 [Primary] |
GS1 | 05705244019904 [Package] Contains: 05705244019898 Package: Outer box [100 Units] In Commercial Distribution |
GS1 | 05705244019911 [Unit of Use] |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-12-06 |
Device Publish Date | 2021-11-26 |
05705244020177 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244020146 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244020054 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244020023 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244019997 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244019966 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244019935 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244019904 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MINIMED 86412764 4738961 Live/Registered |
Medtronic MiniMed, Inc. 2014-10-02 |
![]() MINIMED 75753583 2545204 Dead/Cancelled |
MINIMED INC. 1999-07-19 |
![]() MINIMED 75753448 2426355 Live/Registered |
MEDTRONIC MINIMED, INC. 1999-07-19 |
![]() MINIMED 75753447 2434737 Dead/Cancelled |
MEDTRONIC MINIMED, INC. 1999-07-19 |
![]() MINIMED 75664682 not registered Dead/Abandoned |
American Heritage Life Insurance Company 1999-03-22 |
![]() MINIMED 73461221 1376541 Dead/Cancelled |
Pacesetter Systems, Inc. 1984-01-16 |
![]() MINIMED 73460823 1340467 Live/Registered |
Pacesetter Systems, Inc. 1984-01-13 |