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Micra™ AV2

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
Micra™ AV2 FDA UDI
Generic Name
Intracardiac pacemaker FDA UDI
Device Name
TPS MC2AVR1 MICRA AV2 US FDA UDI
Model / Reference
MC2AVR1 FDA UDI
Description
TPS MC2AVR1 MICRA AV2 US FDA UDI

Identifiers

Primary DI / UDI-DI
00763000078645 FDA UDI
PMA Number
P150033 FDA UDI
FDA Product Code
PNJ FDA UDI
GMDN Term
Intracardiac pacemaker FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.3610 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

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 Conditional FDA UDI

Dimensions & Sizes

Size
Catheter Working Length — 105.0 Centimeter FDA UDI
Catheter Gauge — 23.0 French FDA UDI

Category: Intracardiac pacemaker

Micra™ AV2 by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intracardiac pacemaker.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI d8992780-810d-457c-a795-9f77c1dc01cf 37 fields · synced Jun 8, 2026