MiniMed™ Duo™ Infusion Tubing

GUDID 05705244005259

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

Unomedical A/S

Electric infusion pump administration set, single-use
Primary Device ID05705244005259
NIH Device Record Keyfa10bd3d-4c33-4930-9ad0-043fd6d8b101
Commercial Distribution StatusIn Commercial Distribution
Brand NameMiniMed™ Duo™ Infusion Tubing
Version Model Number5082076-003
Company DUNS306032491
Company NameUnomedical A/S
Device Count10
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx
Phone1-800-646-4633
Emailxx@xx.xx

Device Dimensions

Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter
Length80 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS105705244005259 [Primary]
GS105705244005266 [Package]
Package: Outer box [200 Units]
In Commercial Distribution
GS105705244009806 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FPKTubing, Fluid Delivery

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-15

On-Brand Devices [MiniMed™ Duo™ Infusion Tubing]

05705244005273Single use infusion tubing for subcutaneous infusion. The infusion tubing must be used as descr
05705244005259Single use infusion tubing for subcutaneous infusion. The infusion tubing must be used as descr
05705244005235Single use infusion tubing for subcutaneous infusion. The infusion tubing must be used as descr
05705244005211Single use infusion tubing for subcutaneous infusion. The infusion tubing must be used as descr

Trademark Results [MiniMed]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MINIMED
MINIMED
98731818 not registered Live/Pending
Medtronic MiniMed, Inc
2024-09-04
MINIMED
MINIMED
86412764 4738961 Live/Registered
Medtronic MiniMed, Inc.
2014-10-02
MINIMED
MINIMED
75753583 2545204 Dead/Cancelled
MINIMED INC.
1999-07-19
MINIMED
MINIMED
75753448 2426355 Live/Registered
MEDTRONIC MINIMED, INC.
1999-07-19
MINIMED
MINIMED
75753447 2434737 Dead/Cancelled
MEDTRONIC MINIMED, INC.
1999-07-19
MINIMED
MINIMED
75664682 not registered Dead/Abandoned
American Heritage Life Insurance Company
1999-03-22
MINIMED
MINIMED
73461221 1376541 Dead/Cancelled
Pacesetter Systems, Inc.
1984-01-16
MINIMED
MINIMED
73460823 1340467 Live/Registered
Pacesetter Systems, Inc.
1984-01-13

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.