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CapSure Sense MRI™ SureScan™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
CapSure Sense MRI™ SureScan™ FDA UDI
Generic Name
Endocardial/interventricular septal pacing lead FDA UDI
Device Name
LEAD 407452 MRI US BI MVC RCMRCD FDA UDI
Model / Reference
407452 FDA UDI
Description
LEAD 407452 MRI US BI MVC RCMRCD FDA UDI

Identifiers

Primary DI / UDI-DI
00643169448858 FDA UDI
PMA Number
P830061 FDA UDI
FDA Product Code
DTB FDA UDI
NVY FDA UDI
NVN FDA UDI
GMDN Term
Endocardial/interventricular septal pacing lead FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.3680 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
Length — 52.0 Centimeter FDA UDI

Category: Endocardial/interventricular septal pacing lead

CapSure Sense MRI™ SureScan™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endocardial/interventricular septal pacing lead.

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 c7fb4e8a-0778-4223-8eea-c2af2e87f654 37 fields · synced May 30, 2026