Sprint Quattro Secure S MRI™ SureScan™

FDA UDI

Class III (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: Sprint Quattro Secure S MRI™ SureScan™ FDA UDI
Generic Name: Endocardial defibrillation lead FDA UDI
Device Name: LEAD 693558 SPRINT QUATTRO US MRI FDA UDI
Model / Reference: 693558 FDA UDI
Description: LEAD 693558 SPRINT QUATTRO US MRI FDA UDI

Identifiers

Primary DI / UDI-DI: 00643169690035 FDA UDI
FDA Product Code: DTB FDA UDI
LWS FDA UDI
NVY FDA UDI
GMDN Term: Endocardial defibrillation 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Length — 58.0 Centimeter FDA UDI

Category: Endocardial defibrillation lead

Sprint Quattro Secure S MRI™ SureScan™ by Medtronic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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Manufacturer

Manufacturer: Medtronic, Inc.

Sources (1)

FDA UDI 086b0669-06c6-47b1-adf1-90ed28977805 36 fields · synced May 30, 2026