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Linq Ii™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
LINQ II™ FDA UDI
Generic Name
Implantable cardiac monitor FDA UDI
Device Name
ICM LNQ22 LINQ II USA FDA UDI
Model / Reference
LNQ22 FDA UDI
Description
ICM LNQ22 LINQ II USA FDA UDI

Identifiers

Primary DI / UDI-DI
00763000060374 FDA UDI
510(k) Number
K200795 FDA UDI
FDA Product Code
DSI FDA UDI
MXD FDA UDI
GMDN Term
Implantable cardiac monitor 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

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

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 Conditional FDA UDI

Category: Implantable cardiac monitor

Linq Ii™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable cardiac monitor.

Cleared under the same submission

K200795 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 266d8d55-1584-40de-be45-e4d04f4c720a 36 fields · synced Jun 8, 2026