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MyCareLink™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
MyCareLink™ FDA UDI
Generic Name
Cardiac pulse generator reader, home-use FDA UDI
Device Name
MON 24950LZ MYCARELINK USA MKT MCL FDA UDI
Model / Reference
24950LZ FDA UDI
Description
MON 24950LZ MYCARELINK USA MKT MCL FDA UDI

Identifiers

Primary DI / UDI-DI
00763000304942 FDA UDI
PMA Number
P890003 FDA UDI
FDA Product Code
OSR FDA UDI
NVZ FDA UDI
GMDN Term
Cardiac pulse generator reader, home-use 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

Category: Cardiac pulse generator reader, home-use

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

Similar devices

Also classified as Cardiac pulse generator reader, home-use.

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 ac5867a0-7d7a-49e7-aa5d-4a3fe3dfb4dd 36 fields · synced May 30, 2026