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CareLink SmartSync™ LINQ II™ Insertable Cardiac Monitor (ICM) Application

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
CareLink SmartSync™ LINQ II™ Insertable Cardiac Monitor (ICM) Application FDA UDI
Generic Name
Implantable cardiac device management application software FDA UDI
Device Name
SW D00U024 CARELINK SS LINQ II ICM FDA UDI
Model / Reference
D00U024 FDA UDI
Description
SW D00U024 CARELINK SS LINQ II ICM FDA UDI

Identifiers

Primary DI / UDI-DI
00763000754914 FDA UDI
510(k) Number
K230553 FDA UDI
FDA Product Code
MXD FDA UDI
GMDN Term
Implantable cardiac device management application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Implantable cardiac device management application software

CareLink SmartSync™ LINQ II™ Insertable Cardiac Monitor (ICM) Application by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Implantable cardiac device management application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 6ca747a1-8bab-41a4-9a9b-492ae0a904a5 35 fields · synced May 30, 2026