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MiniMed™ 770G

FDA UDI

Class III (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
MiniMed™ 770G FDA UDI
Generic Name
Ambulatory insulin infusion pump, electronic, software-dosing, scalar algorithm FDA UDI
Device Name
PUMP MMT-1880 770G US PRB FDA UDI
Model / Reference
MMT-1880 FDA UDI
Description
PUMP MMT-1880 770G US PRB FDA UDI

Identifiers

Primary DI / UDI-DI
00763000926113 FDA UDI
PMA Number
P160017 FDA UDI
FDA Product Code
OZP FDA UDI
GMDN Term
Ambulatory insulin infusion pump, electronic, software-dosing, scalar algorithm FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ambulatory insulin infusion pump, electronic, software-dosing, scalar algorithm

MiniMed™ 770G by Medtronic Minimed, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ambulatory insulin infusion pump, electronic, software-dosing, scalar algorithm.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI df66cfbd-bd4d-4e4b-b92f-4bfd4fa172fa 36 fields · synced Jun 1, 2026