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MiniMed® 530G

FDA UDI

Class III (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
MiniMed® 530G FDA UDI
Generic Name
Ambulatory insulin infusion pump, electronic, software-dosing, binary algorithm FDA UDI
Device Name
PUMP MMT-551PNAB PRDGM V3.0 BL US PW FDA UDI
Model / Reference
MMT-551PNAB FDA UDI
Description
PUMP MMT-551PNAB PRDGM V3.0 BL US PW FDA UDI

Identifiers

Primary DI / UDI-DI
00643169736306 FDA UDI
PMA Number
P120010 FDA UDI
FDA Product Code
OZO FDA UDI
GMDN Term
Ambulatory insulin infusion pump, electronic, software-dosing, binary 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, binary algorithm

MiniMed® 530G 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, binary algorithm.

Cleared under the same submission

P120010 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic Minimed, Inc.

Sources (1)

  • FDA UDI cc3442de-01d2-4e06-a91e-eb93059b1815 36 fields · synced Jun 6, 2026