MiniMed® 670G

GUDID 00763000293888

PUMP MMT-1780KR 670G V4.10 MG RECERT

MEDTRONIC MINIMED, INC.

Ambulatory insulin infusion pump, electronic Ambulatory insulin infusion pump, electronic, software-dosing, scalar algorithm Ambulatory insulin infusion pump, electronic, software-dosing, scalar algorithm
Primary Device ID00763000293888
NIH Device Record Keyf0841fac-006a-4259-a57f-4a7d5135ec01
Commercial Distribution StatusIn Commercial Distribution
Brand NameMiniMed® 670G
Version Model NumberMMT-1780KR
Company DUNS849626338
Company NameMEDTRONIC MINIMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Operating and Storage Conditions

Storage Environment HumidityBetween 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment TemperatureBetween -20 Degrees Celsius and 50 Degrees Celsius
Storage Environment HumidityBetween 5 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment TemperatureBetween -20 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000293888 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OZPAutomated insulin dosing device system, single hormonal control

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-04
Device Publish Date2019-10-27

On-Brand Devices [MiniMed® 670G]

00643169946057KIT MMT-1760KPK 670G V3.18 EN MG
00643169946040KIT MMT-1760K 670G REV V3.18 EN MG
00643169939219PUMP MMT-1780KPK 670G V3.18 EN MG
00643169939202PUMP MMT-1780K 670G V3.18 BK SF MG
00763000179649KIT MMT-1760KP 670G 3ML V4.10 EN PW
00763000173043PUMP MMT-1780KP 670G V4.10 SF MG PW
00763000166526PUMP MMT-1780KL 670G V4.10 BK SF MG
00763000157050KIT MMT-1760KPK 670G V4.10 EN MG
00763000075460PUMP MMT-1780KP 670G V3.18 BK SF MG
00763000075453KIT MMT-1760KP 670G 3ML V3.18 BK EN
00763000072537PUMP MMT-1780KL 670G V3.18 BK SF MG
00763000256838PUMP MMT-1780KP 670G V4.11 JBL MG PW
00763000256821PUMP MMT-1780KL 670G V4.11 JBL MG
00763000278427KIT MMT-1760KM 670G V4.11 MG NR
00763000293888PUMP MMT-1780KR 670G V4.10 MG RECERT
00763000293871KIT MMT-1760KR 670G V4.10 MG
00763000283520PUMP MMT-1780KPK 670G V4.11 MG
00763000283513PUMP MMT-1780KL 670G V4.11 JBL MG
00763000283506PUMP MMT-1780KL 670G V4.10 BM MG
00763000283445KIT MMT-1760KPK 670G V4.11 MG
00763000190460PUMP MMT-1780KPK 670G V4.11 EN MG
00763000190453KIT MMT-1760KPK 670G V4.11 EN MG
00763000367084KIT MMT-1760KR 670G V4.11 JBL MG
00763000365929PUMP MMT-1780KM 670G V4.11 JBL MG
00763000365912PUMP MMT-1780KR 670G V4.11 MG JBL RECERT
00763000365882PUMP MMT-1780KL 670G V4.11 JBL MG
00763000367077KIT MMT-1760KM 670G V4.11 MG
00763000395858KIT MMT-1760KPK 670G V4.11 PRB MG
00763000393786PUMP MMT-1780KPK 670G V4.11 PRB MG

Trademark Results [MiniMed]

Mark Image

Registration | Serial
Company
Trademark
Application Date
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.