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Guardian™ Connect App

FDA UDI

Class III (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
Guardian™ Connect App FDA UDI
Generic Name
Patient health record information system application software FDA UDI
Device Name
SFTWR CSS7200 GRDN IOS APP V3.2.1 FDA UDI
Model / Reference
CSS7200 FDA UDI
Description
SFTWR CSS7200 GRDN IOS APP V3.2.1 FDA UDI

Identifiers

Primary DI / UDI-DI
00763000158392 FDA UDI
PMA Number
P160007 FDA UDI
FDA Product Code
MDS FDA UDI
GMDN Term
Patient health record information system application software 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient health record information system application software

Guardian™ Connect App by Medtronic Minimed, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient health record information system application software.

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 edcd043d-415b-4441-8081-689d082e4d3b 35 fields · synced May 30, 2026